Abaloparatide-SC for the Treatment of Post-menopausal Osteoporosis
Abaloparatide-SC is an injectable formulation of abaloparatide developed by Radius Health for the treatment of osteoporosis in post-menopausal women.
Abaloparatide-SC is an injectable formulation of abaloparatide developed by Radius Health for the treatment of osteoporosis in post-menopausal women.
Abatacept (Orencia) was developed by Bristol-Myers-Squibb for the treatment of rheumatoid arthritis (RA). It is a biologic drug which contains a selective co-stimulation modulator.
Abecma (idecabtagene vicleucel) is the first approved CAR T-cell immunotherapy for relapsed or refractory (r/r) multiple myeloma.
Abilify (aripiprazole), an orally administered dopamine partial agonist and a seratonin antagonist, was approved by US Food and Drug Administration (FDA) in November 2002 for the treatment of schizophrenia.
Abraxane (albumin-bound paclitaxel for injectable suspension) is an intravenous injection indicated for the treatment of metastatic pancreatic cancer.
Abrysvo has received a positive opinion from the European Medicines Agency's Committee for Medicinal Products for Human Use.
ACE-031 is an investigational protein therapeutic that is being developed by Acceleron Pharma for the treatment of Du
Developed by Sanofi-Aventis, Acomplia (rimonabant) is a selective CB1 endocannabinoid receptor antagonist indicated for
Roche Pharmaceuticals' Actemra (tocilizumab) was approved as a rheumatoid arthritis treatment in the EU in January 2009
Actonel is targeted for the treatment of osteoporosis in postmenopausal women. It is also indicated for the treatment of osteoporosis in men, to improve BMD and Paget's disease.
Adcetris® (brentuximab vedotin) is a treatment for relapsed or refractory (r/r) Hodgkin’s lymphoma (HL) and anaplastic large cell lymphoma (ALCL).
Adempas (riociguat) is indicated for the treatment of pulmonary arterial hypertension (PAH) and chronic thromboembolic pulmonary hypertension (CTEPH).
Adlyxin (lixisenatide) is an injectable solution developed by Sanofi for the treatment of type 2 diabetes in adults.
Admelog® (insulin lispro) is a rapid-acting human insulin analogue approved as a follow-on product to treat type 1 and type 2 diabetes in adults and paediatric patients aged three years and older.
ADUHELM™ (aducanumab-avwa) is a first-of-its-kind monoclonal antibody indicated for the treatment of Alzheimer’s disease.
ADYNOVI® is an intravenous infusion indicated for the treatment of adults and adolescents with haemophilia A.
Afamelanotide is a photo-protective drug that increases melanin levels in the human skin to gain protection from ultraviolet radiation (UVR) and sunlight.
Afinitor Disperz® (everolimus) is indicated for the treatment of tuberous sclerosis complex (TSC) associated partial-onset seizures in adult and paediatric patients.
Afluria Quadrivalent is an inactivated influenza vaccine developed by Seqirus, which is developed to provide active immunisation against the disease.
Afrezza is a rapid-acting insulin therapy indicated for controlling hyperglycaemia in adult patients with type 1 and type 2 diabetes mellitus.
The FDA approved Agamree for the treatment of DMD in October this year.
Aimovig™ (erenumab) is the first CGRP inhibitor approved for preventive treatment of migraine in adults.
Alecensa (alectinib) is a kinase inhibitor intended for the treatment of patients with anaplastic lymphoma kinase (ALK)-positive non-small cell lung cancer (NSCLC).
Alemtuzumab (marketed as Campath/MabCampath/Lemtrada) is an anti-CD52 monoclonal antibody (MAb) for which Bayer HealthCare holds exclusive global marketing rights. It was licensed in 2001 for the treatment of chronic lymphocytic leukaemia.
Aliqopa (copanlisib) is a novel intravenous phosphatidylinositol-3-kinase (PI3K) inhibitor indicated for the treatment of adult patients with relapsed follicular lymphoma (FL).
Almorexant is the first member of a new class of drugs called orexin receptor antagonists indicated for the treatment of
Alofisel® (formerly Cx601 / darvadstrocel) is the first allogeneic stem cell therapy to be approved for the treatment of complex perianal fistulas in adult patients with Crohn’s disease.
Alprolix [Coagulation Factor IX (Recombinant), Fc Fusion Protein] is an intravenous injection indicated for the control and prevention of bleeding episodes, as well as routine prophylaxis in haemophilia B-affected adults and children aged 12 and above.
Alunbrig (brigatinib) is a tyrosine kinase inhibitor indicated for the treatment of patients with anaplastic lymphoma kinase-positive (ALK+) metastatic non-small cell lung cancer (NSCLC).
Under development by Amira Pharmaceuticals, AM103 is a novel inhibitor of 5-lipoxygenase activating protein (FLAP) that
Amglidia is a hybrid medicine indicated for the treatment of neonatal diabetes mellitus in newborns, infants, and children.
Amondys 45 (casimersen) injection is an antisense oligonucleotide indicated for the treatment of patients with Duchenne muscular dystrophy (DMD). It is the first US Food and Drug Administration (FDA)-approved treatment for patients with DMD with a mutation amenable to skipping exon 45.
Under development by Amarin Corporation, AMR101 is a partially synthetic omega-3 fatty acid-based drug. It contains the
AMVUTTRA™ (vutrisiran) is the first FDA-approved drug to reverse neuropathy impairment in hATTR amyloidosis patients.
AN2728 is an anti-inflammatory drug being developed by Anacor Pharmaceuticals as a treatment for psoriasis.
Anacetrapib (MK-0859) is an orally active cholesteryl ester transfer protein (CETP) inhibitor indicated for the treatment of atherosclerosis.
Andexxa® (coagulation factor Xa recombinant, inactivated-zhzo) is an intravenous infusion indicated for the treatment of patients with factor Xa inhibitor-associated acute major bleeding.
ANKTIVA® is a next-generation immunotherapy to treat BCG-unresponsive non-muscle invasive bladder cancer.
Anoro ellipta (umeclidinium bromide / vilanterol) is a dry powder for inhalation, indicated for the treatment of airflow obstructions in patients suffering from chronic obstructive pulmonary disease (COPD) or emphysema.
Anthim (obiltoxaximab) is an injectable drug developed by Elusys Therapeutics for the treatment of inhalational anthrax caused by bacillus anthracis.
Developed by Arena Pharmaceuticals, APD125 is an oral serotonin antagonist with potential for the treatment of insomnia.
Aphexda™ is a first-of-its-kind product approved for stem cell mobilisation for multiple myeloma in approximately ten years.
Apretude (cabotegravir) is indicated for the treatment of HIV-1 PrEP to minimise the risk of HIV-1 infection.
Aptiom (eslicarbazepine acetate) is a sodium channel inhibitor approved as an adjunctive treatment for partial-onset seizures in the US and Europe.
Arexvy is the world’s first respiratory syncytial virus vaccine to prevent lower respiratory tract disease in older adults.
Ariflo (cilomilast) is an oral selective phosphodiesterase (PDE) IV inhibitor under development by GlaxoSmithKline Pharm
Aristada™ (aripiprazole lauroxil), discovered and developed by Alkermes, is an antipsychotic drug indicated for the treatment of schizophrenia in adults.
Artesunate for Injection is an antimalarial drug indicated for the initial treatment of severe malaria in adult and paediatric patients. It is the only drug in the US to treat the condition.
Arzerra (ofatumumab) is the first-line drug approved for the treatment of chronic lymphocytic leukaemia (CLL).
ASA404 is a vascular disrupting agent (VDA) that was being developed by Antisoma and Novartis as a treatment for a range
ASP-1929 is a first-in-class therapy indicated for the treatment of head and neck squamous cell carcinomas (HNSCC).
Brilinta is an anti-platelet drug which decreases the platelet aggregation and prevents blood clots. It was developed by AstraZeneca for the treatment of acute coronary syndrome (ACS).
Atogepant binds to the CGRP receptor on the brain’s trigeminal nerve and blocks the activation of the migraine.
Aubagio (teriflunomide) is an immunomodulatory agent indicated for the treatment of relapsing forms of multiple sclerosis (MS). It was developed by Genzyme.
Austedo™ (deutetrabenazine) is a vesicular monoamine transporter 2 (VMAT 2) inhibitor indicated for the treatment of chorea associated with Huntington’s disease.
Auvelity™ (dextromethorphan and bupropion) is the first and only oral rapid-acting antidepressant for major depressive disorder.
The product of a joint development programme between Genentech and Roche, Avastin (bevacizumab) is a humanised monoclonal antibody (MAb) directed against vascular endothelial growth factor (VEGF), a pro-angiogenesis factor.
Aveed (testosterone undecanoate) is a testosterone replacement therapy indicated for the treatment of hypogonadism in adult men who are associated with a deficiency or absence of the male hormone testosterone.
Inlyta (axitinib) was developed by Pfizer for treating advanced renal cell carcinoma (ARCC) and hepatocellular carcinoma.
AYVAKIT™ (avapritinib) is the first precision therapy approved for the treatment of adults with unresectable or metastatic gastrointestinal stromal tumours (GISTs) and advanced systemic mastocytosis (ASM).
BALVERSA is available as a round, biconvex, film-coated tablet in 3mg, 4mg, or 5mg strengths.
Bamlanivimab (LY-CoV555) is a neutralising monoclonal antibody intended for the treatment of mild to moderate COVID-19.
Banzel (Rufinamide) was developed in 2004 by Novartis Pharma. It is being manufactured by Eisai in Europe. It is indicated for the treatment of epileptic seizures.
Bavencio® (avelumab) is a human PD-L1 monoclonal antibody indicated for the treatment of metastatic Merkel-cell carcinoma (MCC).
Baxdela™ (delafloxacin) is a fluoroquinolone antibiotic drug indicated for the treatment of adults with acute bacterial skin and skin structure infections (ABSSSI). The drug was discovered and developed by Melinta Therapeutics in partnership with Ligand Pharmaceuticals.
Beleodaq (belinostat) is a histone deacetylase (HDAC) inhibitor indicated for the treatment of relapsed or refractory (R/R) peripheral T-cell lymphoma (PTCL).
Belsomra (suvorexant) is the only approved drug of its kind for treating adult patients suffering from insomnia characterised by difficulty with sleep onset or sleep maintenance. The drug was developed by Merck, Sharp & Dohme Corp.
Benlysta is an investigational human monoclonal antibody drug indicated for treating autoantibody-positive systemic lupu
Beovu® (brolucizumab) is an anti-vascular endothelial growth factor (anti-VEGF) drug indicated for the treatment of neovascular (wet) age-related macular degeneration (AMD).
BESPONSA® is an intravenous infusion indicated for the treatment of adults with relapsed or refractory B-cell precursor acute lymphoblastic leukaemia (ALL).
BESREMi® (ropeginterferon alfa-2B) is a mono-pegylated proline interferon indicated for the treatment of polycythaemia vera.
Bevyxxa (betrixaban) is a drug developed by Portola Pharmaceuticals that is indicated for the prevention and treatment of venous thromboembolism (VTE) in adults.
Discovered and developed by Novartis, Bexsero is a vaccine indicated for the treatment of meningococcal group B (MenB) disease. It is the first and the only Men B vaccine for the protection of all age groups against the disease.
Bifeprunox mesilate was a novel atypical antipsychotic agent under development by Solvay Pharmaceuticals as a treatment
Biktarvy® is a once-daily regimen indicated for the treatment of HIV-1 infection in adults that were previously not treated with anti-retroviral medicines.
Blincyto® (blinatumomab) is a monoclonal antibody indicated as a treatment for relapsed or refractory B-cell precursor acute lymphoblastic leukaemia (ALL) in adults and children.
BNC105, being developed by Adelaide-based Bionomics, is a new kind of drug known as a vascular targeting agent (VDA). As
Victrelis (boceprevir) is an oral HCV protease inhibitor indicated for the treatment of chronic infection with hepatitis
Boostrix is a three-in-one vaccine administered to protect against whooping cough, tetanus and diphtheria. Vaccination is an effective way to protect against them.
Bosutinib is an investigational drug indicated for treating Philadelphia chromosome positive Chronic Myelogenous Leuka
Breo Ellipta (fluticasone furoate and vilanterol inhalation powder) is a dry powder inhaler indicated for the long-term maintenance treatment of airflow obstruction and reduction of exacerbations in patients with chronic obstructive pulmonary disease (COPD).
Brexafemme (ibrexafungerp) is the first FDA-approved oral non-azole treatment for vaginal yeast infections.
Breyanzi is a gene-modified autologous therapy.
Brintellix (vortioxetine) is a new multimodal antidepressant indicated for the treatment major depressive disorder (MDD) in adults.
Briumvi™ is the first and only approved anti-CD20 monoclonal antibody for treating relapsing forms of multiple sclerosis.
Briviact (brivaracetam) was developed by UCB for the treatment of partial onset of seizures in epilepsy patients over the age of 16.
Brukinsa® (zanubrutinib) is a Bruton’s tyrosine kinase (BTK) inhibitor developed by BeiGene.
Bydureon® BCise™ (exenatide extended-release) is an injectable suspension containing a glucagon-like peptide-1 (GLP-1) receptor agonist.
Developed by Amylin Pharmaceuticals, Byetta (exenatide) is a synthetic exendin-4 agent indicated for the treatment of ty
Bylvay™ is indicated to treat skin itching caused by certain inherited liver conditions, PFIC and Alagille syndrome.
Cabenuva is the first and only complete long-acting regimen for the treatment of HIV-1 infection in adults.
Cablivi™ (caplacizumab) is a bivalent anti-Von Willebrand factor (vWF) nanobody indicated for the treatment of adults with acquired thrombotic thrombocytopenic purpura (aTTP).
Cabometyx (cabozantinib) is used for the treatment of patients with advanced renal cell carcinoma (RCC) and hepatocellular carcinoma (HCC).
Calquence® (acalabrutinib) is a bruton tyrosine kinase (BTK) inhibitor indicated for the treatment of adult patients with mantle cell lymphoma (MCL).
Camzyos® (mavacamten) is the only FDA-approved cardiac myosin inhibitor that particularly targets the source of obstructive HCM.
Developed by Pfizer Global Research and Development, capravirine is a Non-Nuclesoide Reverse Transcriptase Inhibitor (NN
Samaritan Pharmaceuticals' caprospinol (SP-233) is an investigational
agent under development for the treatment of Alzh
Carnexiv (carbamazepine) is an injectable formulation developed by Lundbeck for partial, generalised tonic-clonic seizures in adult patients who are unable to temporarily take oral medication.
Carvykti™ (ciltacabtagene autoleucel) is approved by the FDA for the treatment of relapsed or refractory multiple myeloma (RRMM).
Ceftazidime-avibactam is an investigational antibiotic indicated for treatment of patients with complicated urinary tract infections (cUTI) and complicated intra-abdominal infections (cIAI). Actavis is jointly developing the drug in collaboration with AstraZeneca.
The product of a joint development programme between the Swiss pharmaceutical company Basilea Pharmaceutica AG and Cilag AG International (a Johnson & Johnson company), ceftobiprole medocaril (BAL5788) is a novel cephalosporin antibiotic indicated for the treatment of serious bacterial infections in hospitalised patients.
The Celvapan pandemic vaccine is being developed by Baxter International. It was first developed as a mock-up vaccine co
Xpert vanA is a new diagnostic test kit developed by California-based Cepheid for the early and easy detection of vancom
Cerovive, a nitrone-based free radical scavenger indicated for the treatment of acute ischaemic stroke has been disconti
GlaxoSmithKline's (GSK) Cervarix is a prophylactic vaccine currently indicated for the prevention of precancerous cervic
Developed by Alizyme, a specialist biopharmaceutical company in collaboration with Takeda Pharmaceutical, cetilistat (AT
ILUMYA™ (tildrakizumab-asmn) is a subcutaneous infusion indicated for the treatment of adults with moderate-to-severe plaque psoriasis.
CIBINQO (abrocitinib) is a once-daily, oral, prescription medicine to treat moderate to severe atopic dermatitis.
Developed by Solvay Pharmaceuticals, cilansetron is a 5-HT3 antagonist indicated for the treatment of diarrhoea-predomin
CIMZIA® (certolizumab pegol) is a subcutaneous infusion indicated for the treatment of adults with moderate-to-severe plaque psoriasis.
Cinqair is an injectable formulation of reslizumab developed by Teva Pharmaceuticals for the treatment of severe asthma and eosinophilic phenotype in adults.
Schizophrenia is a chronic and debilitating mental disorder that impacts the way an individual thinks, feels, and acts.
Columvi is a bispecific antibody, fixed-duration treatment for relapsed or refractory diffuse large B-cell lymphoma.
Contrave (Bupropion / naltrexone) is a drug indicated for treating obesity. The drug was developed by Orexigen Therapeutics.
COPIKTRA (duvelisib) is a dual phosphoinositide 3-kinase (PI3K) inhibitor indicated for the treatment of patients with chronic lymphocytic leukaemia (CLL), small lymphocytic lymphoma (SLL) or follicular lymphoma (FL).
Corifact is an intravenous drug indicated for the treatment of bleeding disorder in patients with factor XIII deficien
Corlanor (ivabradine) is an oral medication approved to reduce the risk of hospitalisation for worsening heart failure in patients facing chronic heart failure risk due to the lower-left part of the heart not contracting well.
COSELA™ (trilaciclib) is the first approved myeloprotection therapy indicated to reduce the occurrence of chemotherapy-induced bone marrow suppression in adult patients.
Cosentyx is the only treatment approved in an IV formulation that specifically targets and blocks interleukin-17A (IL-17A).
COVAXIN™ (BBV152) is the first Covid-19 vaccine developed completely in India.
Cresemba (isavuconazonium sulphate) is an antifungal drug indicated for the treatment of invasive aspergillosis and invasive mucormycosis, which is also known as zygomycosis.
Crysvita® (burosumab-twza) is a fibroblast growth factor 23 (FGF23) blocking antibody indicated for the treatment of X-linked hypophosphatemia (XLH) in adults and children.
Cuvposa (Glycopyrrolate) is the first and only approved drug for controlling drooling in patients aged between three
CXL-1020 is an investigational therapeutic agent being developed for treating patients with acute decompensated heart fa
Cymbalta (Duloxetine hydrochloride) is indicated for treating chronic musculoskeletal pain as a result of osteoarthritis
Cyramza (ramucirumab) is a human monoclonal antibody for the treatment of Gastric cancer.
Cystaran (cysteamine hydrochloride) is a cystine-depleting agent indicated for the treatment of cystinosis.
Cytalux is the first intraoperative fluorescent imaging drug that helps in identifying ovarian cancer lesions during surgery.
Daklinza (daclatasvir), an NS5A replication complex inhibitor, is the first 12-week, all-oral therapy indicated for use with sofosbuvir, for the treatment of hepatitis C (HCV) genotype 3 infections.
Daliresp (Roflumilast) is an oral tablet that is proved to reduce the risk of exacerbations in patients suffering from
Originally developed by Vicuron Pharmaceuticals (which was subsequently acquired by Pfizer and then Durata Therapeutics)
DANYELZA® (naxitamab-gqgk) is a humanised immunotherapy indicated in combination with granulocyte-macrophage colony-stimulating factor (GM-CSF) for the treatment of high-risk neuroblastoma (HR-NB).
Darapladib is a selective LpPLA2 inhibitor under development by GlaxoSmithKline (GSK). The drug is targeted at coronary
Darzalex (daratumumab) is the world's first human anti-CD38 monoclonal antibody (mAb) approved for the treatment of patients with multiple myeloma.
DARZALEX FASPRO® (daratumumab and hyaluronidase-fihj) is the first subcutaneous therapy approved for the treatment of newly diagnosed light chain (AL) amyloidosis in adult patients.
Dasatinib is a new, oral small-molecule tyrosine kinase inhibitor (TKI) developed by Bristol Myers Squibb for the trea
Defitelio (defibrotide sodium) is an injectable drug developed by Jazz Pharmaceuticals, for the treatment of hepatic veno-occlusive disease (VOD) also known as sinusoidal obstruction syndrome, in adults and children with renal or pulmonary dysfunction following hematopoietic stem cell transplantation (HSCT).
Delstrigo™ is a fixed-dose combination tablet of antiretroviral drugs doravirine, lamivudine, and tenofovir disoproxil fumarate indicated for the treatment of human immunodeficiency virus (HIV) 1 infection.
Descovy (emtricitabine200mg/tenofovir alafenamide25mg, F/TAF) is developed by Gilead sciences for the treatment of HIV-1 infection in adults and children above 12 years of age.
Dificid (fidaxomicin) is the first in a new class of antibiotics developed by Optimer Pharmaceuticals to treat Clostridi
Dimebon (latrepirdine) is an investigational compound indicated for the treatment of Alzheimer's and Huntington's diseas
Dinutuximab beta is an anti-GD2 monoclonal antibody indicated for the treatment of neuroblastoma in patients aged one year and above.
Doptelet® (avatrombopag) is one of the first thrombopoietin (TPO) receptor agonists to be approved in the US for the treatment of thrombocytopenia in adult patients with chronic liver disease (CLD).
Doripenem is part of Johnson &' Johnson's anti-infective R&D portfolio following the acquisition of Peninsula Ph
Dovato® (dolutegravir/lamivudine) is a two-drug regimen indicated for the treatment of human immunodeficiency virus type 1 (HIV-1) in adults.
Duaklir Genuair (aclidinium bromide / formoterol fumarate) is an inhalation powder indicated as a maintenance bronchodilator treatment for chronic obstructive pulmonary disease (COPD).
Dulera (mometasone furoate and formoterol fumarate dihydrate) is a new fixed-dose combination inhaler for the treatment of asthma.
Dupixent (dupilumab) is the first targeted treatment for children as young as six months old with severe atopic dermatitis.
Durlaza (aspirin) is a non steroidal anti-inflammatory drug indicated for the prevention of thrombotic events in patients with cardiovascular disease (CVD).
Duvyzat™ (givinostat) is the first non-steroidal drug approved to treat all genetic variants of Duchenne muscular dystrophy (DMD).
Duzallo (allopurinol and lesinurad) is indicated for the treatment of hyperuricemia associated with uncontrolled gout. It contains urate transporter-1 (URAT-1) inhibitor blended with xanthine oxidase inhibitor (XOI).
Dysport (abobotulinumtoxinA) is an injectable formulation developed by Ipsen Biopharmaceuticals for the treatment of lower limb spasticity in paediatric patients aged two years or older.
Ebanga (ansuvimab-zykl) is a Zaire ebolavirus glycoprotein (EBOV GP)-directed human monoclonal antibody for the treatment of Zaire ebolavirus infection in adult and paediatric patients.
Edarbi (Azilsartan medoxomil) was developed by Takeda Pharmaceuticals for the treatment of hypertension in adults.
Lixiana (edoxaban) is an oral anticoagulant developed by Daiichi Sankyo, a pharmaceutical company based in Japan. It is
Edurant (rilpivirine) is an antiviral drug indicated for treatment-naive adults with HIV-1 infection.
Elacytarabine (CP-4055) is a lipid-conjugated version of cytarabine, an anti-cancer agent drug approved for the treatmen
AbbVie acquired ImmunoGen in February 2024, which added ELAHERE to its portfolio.
Elelyso (taliglucerase alfa) is an intravenous drug indicated for the treatment of type one Gaucher disease. The drug was jointly developed by Protalix BioTherapeutics and Pfizer.
Elevidys (delandistrogene moxeparvovec) is the first gene therapy approved to treat Duchenne muscular dystrophy in children.
Eliquis (apixaban) is an anticoagulant drug that was jointly developed by Bristol-Myers Squibb and Pfizer.
Eloctate is a drug approved for the control and prevention of bleeding episodes in children and adult haemophilia A patients.
Elotuzumab (HuLuc63) is an anti-CS1 humanised monoclonal antibody (MAb) developed by PDL Biopharma. In December 2008 PDL
ELREFXIO™ (elranatamab) is a targeted immunotherapy to treat adult patients with relapsed and refractory multiple myeloma (RRMM).
Elzonris™ (tagraxofusp-erzs) is an interleukin-3 receptor alpha chain (CD123) directed cytotoxin that is indicated for the treatment of blastic plasmacytoid dendritic cell neoplasm (BPDCN) in adults and paediatric patients.
Emflaza™ (deflazacort) is the first glucocorticoid drug approved in the US for treatment of patients aged two years and older suffering from duchenne muscular dystrophy (DMD).
EMPAVELI™ (pegcetacoplan) is the first and only targeted complement component 3 (C3) therapy indicated for the treatment of paroxysmal nocturnal haemoglobinuria (PNH) in adults.
Empliciti (elotuzumab) is an immunostimulatory antibody indicated for the treatment of multiple myeloma.
Enbrel is an immunosuppressant that inhibits the production of tumour necrosis factor (TNF) in patients suffering from r
Endari™ is an orally administered powdered form of amino acid L-glutamine indicated for the treatment of sickle-cell disease.
Enhertu is a HER2-directed antibody-drug conjugate jointly developed by AstraZeneca and Daiichi Sankyo.
Enjaymo™ (sutimlimab-jome) is a classical complement inhibitor that works by inhibiting the haemolysis of red blood cells.
Enspryng™ (satralizumab-mwge) is the first and only US Food and Drug Administration (FDA)-approved subcutaneous therapy indicated for the treatment of neuromyelitis optica spectrum disorder (NMOSD) in anti-aquaporin-4 (AQP4) antibody-positive adult patients.
Discovered by Bristol-Myers Squibb (BMS), Entecavir / Baraclude is an antiviral drug for treating chronic Hepatitis B.
Entresto (sacubitril/valsartan) is an angiotensin II receptor blocker indicated for the treatment of chronic heart failure.
Positive clinical trail results for Entyvio have led to its approval in both the US and EU markets.
Epanova (omega-3-carboxylic acids) is indicated for the treatment of adult patients with severe hypertriglyceridaemia.
Epclusa (Sofosbuvir/ Velpatasvir) is an oral formulation developed by Gilead Sciences for the treatment of 1-6 chronic hepatitis C virus (HCV) infection.
EPIDIOLEX® is a cannabidiol (CBD) based drug indicated for the treatment of seizures associated with Lennox-Gastaut Syndrome (LGS) and Dravet Syndrome (DS).
Epkinly™ (epcoritamab-bysp) is the first bispecific antibody to treat adults with diffuse large B-cell lymphoma.
Erbitux is a chimaeric monoclonal antibody (MAb) that is specific for the epidermal growth factor receptor (EGFR). A new
Erivedge (vismodegib) is a Hedgehog pathway inhibitor indicated for the treatment of advanced basal cell carcinoma (BCC) in adults.
Erleada™ (apalutamide) is an androgen receptor inhibitor indicated for the treatment of patients with non-metastatic castration-resistant prostate cancer (NM-CRPC).
Erwinaze (asparaginase Erwinia chrysanthemi) is indicated for the treatment of acute lymphoblastic leukaemia (ALL). It is manufactured by EUSA Pharma.
Eskata® (hydrogen peroxide) is a topical, non-invasive treatment for raised seborrheic keratoses (SK) in adults.
Esperoct® (turoctocog alfa pegol) is a recombinant factor indicated for the treatment of haemophilia A in adults and children.
Developed by US biopharmaceutical company Esperion Therapeutics, ETC-216 is a synthetic variant of high-density lipoprot
Eviplera is a single-pill regimen targeted at human immunodeficiency virus-1 (HIV-1). It combines the active substances emtricitabine, rilpivirine and tenofovir disoproxil.
Evotaz (atazanavir and cobicistat) is a protease inhibitor indicated for the treatment of HIV-1 infection in adults.
Evrysdi is the first and only oral medication indicated for the treatment of SMA in patients.
Evusheld is a long-acting antibody combination therapy for the pre-exposure prevention of Covid-19 in high-risk patients.
Exanta (ximelagatran) is an oral Direct Thrombin Inhibitor (DTI) under development by AstraZeneca. As the first fixed-do
Exjade (deferasirox) is an oral iron chelator developed and manufactured by Novartis. It is indicated for the treatment of iron overload in patients with non-transfusion-dependent thalassemia (NTDT) syndromes.
Exkivity is the first and only oral therapy indicated for non-small cell lung cancer with EGFR exon 20 insertion mutations.
Exondys 51 (eteplirsen) is an injectable solution developed by Sarepta Therapeutics.
Exparel is a non-opioid analgesic, developed to provide postsurgical pain relief. It is a long acting liposome injection of bupivacaine, a drug widely used to treat postsurgical pain.
The product of a joint development programme between Aventis and Pfizer, Exubera is an inhaled short-acting insulin prep
Eylea (aflibercept), a recombinant fusion protein, was developed for the treatment of patients with wet age-related macular degeneration (AMD).
Fabhalta (iptacopan) is the first oral monotherapy indicated for the treatment of adults with paroxysmal nocturnal hemoglobinuria (PNH).
The product of a joint development programme between Pfizer and Ligand Pharmaceuticals, Fablyn, formerly Oporia (lasofoxifene) is a selective oestrogen receptor modulator (SERM).
Developed by Acorda Therapeutics and manufactured by Elan Corporation, fampridine-SR (now referred to as AMPYRA) is a se
Farydak (panobinostat, previously known as LBH589) is a histone deacetylase (HDAC) inhibitor indicated for the treatment of patients with multiple myeloma.
Fasenra (benralizumab) is a monoclonal antibody (mAb) indicated for the treatment of severe eosinophilic asthma in patients aged 12 years and older.
Faslodex (fulvestrant) is an oestrogen receptor antagonist indicated for the treatment of locally advanced or metastatic breast cancer.
FETROJA® (cefiderocol) is the first approved siderophore cephalosporin antibacterial drug.
Fetzima (levomilnacipran) is an antidepressant indicated for treatment of adult patients suffering from major depressive disorder (MDD).
Discovered and developed by Novo Nordisk, Fiasp® (insulin aspart) is a fast-acting insulin analogue indicated for the treatment of adults with Type 1 and Type 2 diabetes.
Filspari (sparsentan) is the first approved non-immunosuppressive therapy for reducing proteinuria in IgA nephropathy.
Fingolimod (branded Gilenya) is an innovative treatment for multiple sclerosis (MS) under development by Novartis. The d
FINTEPLA® (fenfluramine) is indicated to treat seizures associated with Dravet syndrome and Lennox-Gastaut syndrome.
FIRAZYR (Icatibant) is a drug developed and manufactured by Jerini, which was taken over by Shire Pharmaceuticals in 2008. The drug is indicated for the treatment of Hereditary Angioedema (HAE).
Firdapse® (amifampridine) is one of the first drugs to be approved for the treatment of Lambert-Eaton myasthaenic syndrome (LEMS) in adults.
Alzheimer's disease (AD) is the most common type of dementia, which severely impacts the intellectual abilities of a
Flucelvax, developed by Novartis in association with the US Department of Health and Human Services, is a vaccine that provides protection against seasonal influenza for adult patients aged 18 years and above.
NexBio, a US start-up biopharmaceutical company that specialises in developing antiviral agents, has pioneered the development of Fludase (DAS181).
FluLaval is an influenza vaccine that was approved by the US FDA on 23 July 2010, for use on people who are 18 years and
Myriad Pharmaceuticals' Flurizan (tarenflurbil) is a selective amyloid lowering agent under development for the treatmen
Flutiform (fluticasone proprionate and formoterol fumarate) is a combination therapy used for the treatment of asthma.
Forxiga® (dapagliflozin) is approved for the treatment of paediatric type 2 diabetes, chronic heart failure and chronic kidney disease.
FOTIVDA® (tivozanib) is an oral tyrosine kinase inhibitor approved for the treatment of renal cell carcinoma (RCC) in adult patients.
FRUZAQLA® (fruquintinib) is an oral targeted therapy indicated for adult patients with metastatic colorectal cancer (mCRC).
Fulyzaq (crofelemer) is an anti-infective drug which is derived from a botanical source. It is indicated for the treatment of non-infectious diarrhoea in HIV / AIDS patients who are on anti-retroviral therapy (ART).
Fycompa (perampanel / E2007) is an AMPA-type glutamate receptor antagonist indicated for the treatment of epilepsy. It was developed by Japan-based healthcare company Eisai.
Gaboxadol is a direct-acting gamma-amino butyric acid (GABA)A agonist under development by Danish pharmaceutical company
Galafold™ (migalastat) is indicated for the treatment of adult patients aged 16 years and older with Fabry disease.
AstraZeneca's, Galida (tesaglitazar) is a dual-acting oral Peroxisome Proliferator-Activated Receptor (PPAR) agonist tha
Gamifant® (emapalumab-lzsg) is an interferon-gamma (IFNγ) blocking antibody indicated for the treatment of primary haemophagocytic lymphohistiocytosis (HLH) in paediatric and adult patients.
Gardasil 9 (human papillomavirus 9-valent vaccine, recombinant) is indicated for the prevention of cancers caused by some types of human papillomavirus (HPV).
Gattex (teduglutide) is a subcutaneous injection indicated for the treatment of adult patients with short bowel syndrome (SBS). The drug was developed and manufactured by NPS Pharmaceuticals in association with Takeda Pharmaceuticals.
Gavreto™ (pralsetinib) is a targeted therapy indicated for the treatment of metastatic rearranged during transfection (RET) fusion-positive non-small cell lung cancer (NSCLC), diagnosed by a US Food and Drug Administration (FDA)-approved test, in adult patients.
Gazyva (obinutuzumab / GA101) is a monoclonal antibody indicated for the treatment of chronic lymphocytic leukaemia (CLL).
GEMTESA’s long-term safety, tolerability, and efficacy in adults with OAB was evaluated in a 40-week Phase III EMPOWUR extension study.
Gilotrif (afatinib) is an orally administered drug that is indicated as the first-line treatment for metastatic non-small cell lung cancer (NSCLC) patients with epidermal growth factor receptor (EGFR) mutations.
Givlaari™ (givosiran) is the first aminolevulinic acid synthase 1 (ALAS1)-targeting RNAi drug indicated for the treatment of acute hepatic porphyria (AHP) in adults.
Glatopa (glatiramer acetate injection, formerly M356) is the first substitutable generic drug approved for the treatment of relapsing-remitting multiple sclerosis (RRMS).
GLS-5700 is a synthetic vaccine being developed by Inovio Pharmaceuticals and GeneOne Life Sciences to prevent and treat infections caused by the Zika virus.
Glybera (alipogene tiparvovec) is a gene therapy indicated for the treatment Lipoprotein Lipase Deficiency (LPLD). It was developed by Amsterdam Molecular Therapeutics (AMT), which was acquired by uniQure in April 2012.
GRNOPC1 is an indicative stem cell therapy developed by Geron for the treatment of spinal cord injuries (SCI).
Haegarda® (C1 Esterase Inhibitor) a subcutaneous prophylactic therapy indicated for the prevention of hereditary angioedema (HAE) attacks in adolescent and adult patients.
The NMPA granted conditional approval for Haiyitan in China for NSCLC patients with METex14 skipping mutations in 2023.
Halaven is a non-taxane drug developed by Eisai Co. for the treatment of metastatic breast cancer.
Halaven (eribulin mesylate) is an injectable chemotherapy drug developed by Eisai for the treatment of unresectable or metastatic liposarcoma patients that previously received anthracycline-based chemotherapy.
Developed by Gilead Sciences, Harvoni (ledipasvir/sofosbuvir) is the first combination pill approved for the treatment of adult patients with chronic hepatitis C genotype 1 infection.
Hemlibra® (emicizumab-kxwh) is an antibody indicated to reduce the frequency of bleeding episodes in adults and children with haemophilia A with factor VIII inhibitors.
Herzuma® (trastuzumab biosimilar / CT-P6) is indicated for the treatment of human epidermal growth factor receptor 2 (HER2) overexpressing breast cancer and metastatic gastric cancer.
Hetlioz (tasimelteon) is the first and only drug approved in the European Union (EU) for non-24-hour sleep-wake disorder (Non-24).
Hizentra® (immune globulin subcutaneous 20% liquid) is a subcutaneous infusion indicated for the treatment of patients with chronic inflammatory demyelinating polyneuropathy (CIDP).
Horizant is a non-dopaminergic therapy indicated for the treatment of restless legs syndrome (RLS). It was developed by XenoPort and is marketed by GSK in the US.
HUMIRA is the only subcutaneous therapy approved by the US Food and Drug Administration (FDA) for the treatment of ulcerative colitis in paediatric patients aged five years and above.
Humira (adalimumab) is a monoclonal antibody indicated for the treatment of more than ten indications, including rheumatoid arthritis (RA), juvenile idiopathic arthritis (JIA), psoriatic arthritis, ankylosing spondylitis, Crohn’s disease, ulcerative colitis, plaque psoriasis, hidradenitis suppurativa (HS), and uveitis.
Hycamtin is an anti-cancer drug developed by GlaxoSmithKline (GSK) as a treatment for relapsed small cell lung cancer (S
Hydroxychloroquine, marketed by Sanofi under the trade name Plaquenil, is primarily indicated for the treatment of malaria, discoid and systemic lupus erythematosus, and rheumatoid arthritis.
HYQVIA® can treat primary immunodeficiency (PI) and chronic inflammatory demyelinating polyneuropathy (CIDP).
Ibrance (palbociclib) is an oral formulation developed by Pfizer for the treatment of metastatic breast cancer in women with disease progression post endocrine therapy.
Iclusig (ponatinib) is indicated for the treatment of chronic myeloid leukaemia (CML) and Philadelphia chromosome-positive acute lymphoblastic leukaemia (Ph+ALL). The drug is discovered, developed and marketed by Ariad Pharmaceuticals.
Idelvion (Coagulation Factor IX (Recombinant), Albumin Fusion Protein) is an injectable formulation developed by CSL Behring, for the treatment of haemophilia B in children and adults.
Idhifa (enasidenib) is an isocitrate dehydrogenase 2 (IDH2) enzyme inhibitor indicated for the treatment of adult patients with relapsed or refractory acute myeloid leukaemia (AML).
The product of a joint development programme between Sanofi-Aventis (formerly Sanofi-Synthelabo) and Organon, Idraparinux is a new addition to the family of anticoagulant drugs.
Ilaris (canakinumab) is a subcutaneous injection indicated for the treatment of systemic juvenile idiopathic arthritis (SJIA).
Iloperidone is a dual-acting dopamine and serotonin receptor antagonist, developed originally by Titan Pharmaceuticals a
Iluvien is indicated for the treatment of diabetic macular oedema, an eye disease that affects the retina.
Imbruvica (ibrutinib) is an oral Bruton's tyrosine kinase (BTK) inhibitor indicated for the treatment of mantle cell lymphoma (MCL) patients that previously received at least one therapy.
IMCIVREE® (setmelanotide) is the first approved treatment for managing weight in Bardet-Biedl syndrome patients.
IMDELLTRA™ (tarlatamab) is the first T-cell engager therapy approved to treat extensive-stage small cell lung cancer (ES-SCLC).
Imfinzi™ (durvalumab) is a monoclonal antibody (mAb) indicated for the treatment of metastatic urothelial carcinoma (mUC).
Developed by Amgen, Imlygic (talimogene laherparepvec) is the first injectable formulation of altered herpes simplex virus type 1 for the treatment of cutaneous, subcutaneous and nodal lesions in patients with melanoma recurrence after initial surgery.
Inbrija is indicated for OFF episodes in adults with Parkinson’s disease treated with carbidopa/levodopa medicine.
Under development by Incyte Corporation, INCB9471 is an experimental small molecule drug indicated for the treatment of
Incivek (telaprevir) is a protease inhibitor used for treating hepatitis C infections in liver patients.
IncruseTM (unmeclidinium) Ellipta is the first approved anticholinergic indicated as a maintenance treatment to relieve the symptoms of chronic obstructive pulmonary disease (COPD) in adult patients.
Merck's Crixivan (indinavir sulphate) is a first-generation HIV-protease inhibitor. Drugs such as indinavir have demonst
Sanofi Pasteur's Influenza A (H1N1) 2009 Monovalent Vaccine for 2009 Influenza A (H1N1) or swine flu is one of the f
Ingrezza (valbenazine) is first and only US Food and Drug Administration (FDA) approved vesicular monoamine transporter 2 (VMAT2) inhibitor indicated for the treatment of adults with Tardive dyskinesia (TD).
INMAZEB™ (atoltivimab, maftivimab, and odesivimab) is the first antiviral antibody therapeutics approved for the treatment of Zaire ebolavirus infection in adults and children, including newborns whose mothers tested positive for the infection.
Inspra (eplerenone) is indicated for the treatment of chronic heart failure. It was developed by Pharmacia Corporation,
Intermezzo is a formulation of zolpidem that is indicated for the treatment of insomnia or sleeping disorders. The drug
Invega Hafyera™ (paliperidone palmitate) is a long-acting atypical antipsychotic drug indicated for the treatment of schizophrenia.
Invega Trinza (paliperidone palmitate), an atypical antipsychotic, is a three-month injection that is the first, and only, four-times-a-year drug indicated to treat schizophrenia .
Developed by Janssen Pharmaceuticals, Invokamet XR (Canagliflozin / Metformin Hydrochloride Extended Release) is indicated for the treatment of Type 2 diabetes in adults.
Invokana (canagliflozin) is indicated to improve glycemic control in adults with type 2 diabetes, along with diet and exercise. It was first developed by Mitsubishi Tanabe Pharma Corporation in Japan and later licensed to Janssen Pharmaceuticals.
Iomab-B is a radio-immunotherapeutic drug developed by Actinium Pharmaceuticals for treatment of refractory and relapsed acute myeloid leukaemia in elderly patients.
Iqirvo is available for oral administration as round, orange-coloured, film-coated tablets in a dosage strength of 80mg.
Istaroxime is an investigational drug for acute decompensated heart failure under development by Debiopharm of Switzerla
Isturisa® (osilodrostat) is the first cortisol synthesis inhibitor indicated for the treatment of Cushing's disease in adult patients, who are ineligible or failed pituitary surgery.
Iwilfin is the first and only oral maintenance therapy for high-risk neuroblastoma approved by the FDA.
Bristol-Myers Squibb's (BMS) ixabepilone (epothilone B) is a new chemotherapeutic agent that is currently in development
Ixinity (coagulation factor IX (recombinant)) is an intravenous injection containing recombinant human coagulation factor IX that is indicated for the control and prevention of bleeding episodes in patients suffering from haemophilia B.
Izervay is available as a clear to slightly opalescent, colourless to slightly yellow solution.
Jakafi (ruxolitinib) is an oral janus kinase (JAK) inhibitor indicated for the treatment of myelofibrosis. It was developed by Incyte Corp in collaboration with Novartis.
Januvia (sitagliptin phosphate) is an antihyperglycaemic drug containing an orally active inhibitor of the dipeptidyl pe
Jardiance® (empagliflozin) is an SGLT2 inhibitor indicated to treat heart failure in adults with reduced ejection fraction.
Jardiance is available as a film-coated, pale-yellow-coloured tablet in 10mg and 25mg strengths for oral administration.
Jaypirca™ is a first-of-a kind BTK inhibitor for the treatment of mantle cell lymphoma in previously treated patients.
Jemperli is the first anti-PD-1 therapy for the treatment of certain types of endometrial cancer in Europe.
Jesduvroq (daprodustat) is the first oral treatment for anaemia caused by chronic kidney disease in adults undergoing dialysis.
Jetrea (ocriplasmin) is a pharmacological agent developed by ThromboGenics, for the treatment of Symptomatic Vitreomacular Adhesion (VMA).
Juluca® (Dolutegravir and Rilpivirine) is a two-drug regimen indicated for the maintenance treatment of HIV-1 infection in adults.
Juxtapid (lomitapide) is developed and manufactured by Aegerion Pharmaceuticals for the treatment of patients affected with homozygous familial hypercholesterolemia (HoFH).
JYNARQUE™ (tolvaptan) is indicated for the treatment of autosomal dominant polycystic kidney disease (ADPKD).
JYNNEOS™ is a non-replicating vaccine indicated for smallpox and monkeypox disease prevention in adults aged 18 years and older.
Kadcyla (trastuzumab emtansine) is an antibody drug conjugate indicated for the treatment of HER2-positive metastatic breast cancer (mBC). The drug has been developed by Genentech (a member of the Roche Group).
Kalbitor (ecallantide) is a drug developed by US-based Dyax Corp for the treatment of hereditary angioedema (HAE).
Kalydeco (Ivacaftor / VX-770) is a cystic fibrosis transmembrane conductor regulator (CFTR) potentiator indicated for the treatment of cystic fibrosis (CF).
KamRAB/KedRAB™ is a human rabies immunoglobulin (HRIG) indicated for the treatment of passive, transient post-exposure prophylaxis (PEP) of rabies infection. The drug was jointly developed by Kamada and Kedrion Biopharma.
Kanuma™ (sebelipase alfa) is an enzyme replacement therapy (ERT) for the treatment of patients of all ages with lysosomal acid lipase deficiency (LAL-D).
Kengreal (cangrelor) is the first and only intravenous anti-platelet agent indicated as an adjunct to percutaneous coronary intervention (PCI) for reducing thrombotic events.
KERENDIA® is the first, nonsteroidal mineralocorticoid receptor antagonist for diabetes-related chronic kidney disease.
Kesimpta® (ofatumumab) is the first and only self-administered, targeted B-cell therapy indicated for the treatment of patients with relapsing multiple sclerosis (RMS) including clinically isolated syndrome (CIS), relapsing-remitting (RRMS), and active secondary progressive multiple sclerosis (SPMS).
Keveyis (dichlorphenamide) is the first medicine indicated for the treatment of primary hyperkalemic and hypokalemic periodic paralysis, which are a group of rare hereditary disorders that cause occasional episodes of muscle weakness or paralysis.
Kevzara® (sarilumab) is a human monoclonal antibody indicated for the treatment of adult patients with moderate-to-severely active rheumatoid arthritis (RA).
Keytruda (pembrolizumab) is an anti-programmed death receptor-1 (PD-1) immunotherapy developed by Merck to treat melanoma.
Kineret (anakinra) is a recombinant protein drug which was originally discovered and developed by Amgen. The drug was later licensed to Swedish Orphan Biovitrum (Sobi) in December 2008.
Formerly known as LEE011, Kisqali® (ribociclib) is a cyclin-dependent kinase 4 and 6 (CDK4/6) inhibitor indicated for the treatment of hormone receptor positive, human epidermal growth factor receptor 2 negative (HR+/HER2-) metastatic breast cancer in post-menopausal women.
Kisunla™ (donanemab-azbt) is an amyloid plaque-targeting therapy, developed by Eli Lilly, to treat early Alzheimer's disease.
Korlym (mifepristone) is a glucocorticoid receptor blocker indicated for the control of high blood sugar levels in adult patients suffering from endogenous Cushing's syndrome.
Korsuva (difelikefalin) is the first US FDA-approved treatment for moderate-to-severe pruritus in adult patients on haemodialysis.
Koselugo® (selumetinib) is the first FDA-approved drug indicated for the treatment of neurofibromatosis type 1 (NFI), a rare and incurable genetic condition, developed and commercialised globally by AstraZeneca and Merck (MSD) under a licensing agreement.
Kovaltry (Anti haemophilic Factor VII (Recombinant)) is developed by Bayer as the treatment for children and adult patients with haemophilia A.
Krazati™ (adagrasib) is a targeted treatment for advanced non-small cell lung cancer (NSCLC) with KRASG12C mutation.
KRX-0401 (perifosine) is a potential oral anti-cancer agent that suppresses the pathways associated with the programmed
Kymriah (tisagenlecleucel) is the first FDA-approved CAR-T therapy indicated for treating ALL.
KYNMOBI is the first and only sublingual therapy indicated for the on-demand treatment of OFF episodes in Parkinson's disease.
Kyprolis (carfilzomib), developed and manufactured by Onyx Pharmaceuticals, is a proteasome inhibitor indicated for the treatment of the patients with multiple myeloma.
Lamictal XR (lamotrigine), developed by GlaxoSmithKline, is an approved treatment for epilepsy and bipolar I disease. Th
Lampit® (nifurtimox) is an antiprotozoal medication indicated for the treatment of Chagas disease (American Trypanosomiasis) in paediatric patients from birth to less than 18 years of age and weighing at least 2.5kg.
Lamzede® (velmanase alfa) is one of the first enzyme replacement therapies indicated for the treatment of non-neurological symptoms of patients with mild-to-moderate alpha‑mannosidosis.
Developed by Eli Lilly and Company, Lartruvo (olaratumab) in combination with doxorubicin is indicated for the treatment of soft tissue sarcoma (STS) in adult patients. The drug is available as a 10mg/ml injection.
Latuda (lurasidone HCl) is indicated for the treatment of schizophrenia. The drug was developed by Sunovion Pharmaceut
Lenvima™ (lenvatinib mesylate) is a multiple receptor tyrosine kinase (RTK) inhibitor indicated for the treatment of thyroid cancer.
Leqembi™ is the second FDA-approved anti-amyloid antibody for Alzheimer disease, after Biogen’s aducanumab.
Patients need to be administered two maintenance doses of the drug a year via syringe, following an initial dose and another at three months.
In March 2009, the US Food and Drug Administration (FDA) approved the supplemental new drug application (sNDA) of Forest
Libtayo (cemiplimab-rwlc) is an advanced fully human monoclonal antibody indicated for the treatment of metastatic or locally advanced cutaneous squamous cell carcinoma (CSCC) in patients ineligible to undergo curative surgery or radiation therapy.
Developed by the German pharmaceutical company, Merckle GmbH, together with EuroAlliance partners Alfa Wassermann and La
Linzess (linaclotide) is a guanylate cyclase-C (GC-C) receptor agonist co-developed by AbbVie and Ironwood Pharmaceuticals.
Lipaglyn (saroglitazar) is approved for the treatment of hypertriglyceridaemia in type 2 diabetes.
Lipitor (Atorvastatin) is a statin class drug indicated for reducing high cholesterol levels in the blood, which helps prevent cardiovascular diseases. It is manufactured by Pfizer.
Under development by Pfizer, torcetrapib is a member of the cholesteryl ester transfer protein (CETP) inhibitor class of
Liptruzet (ezetimibe and atorvastatin) is a combination drug indicated to reduce elevated low-density lipoprotein (LDL) cholesterol in patients suffering from hyperlipidaemia disorder.
Under development by Novo Nordisk, liraglutide is a member of a new class of antidiabetic medications called GLP-1 analo
Livdelzi® (seladelpar) received accelerated approval from the US FDA in August 2024 for treating primary biliary cholangitis.
Livmarli™ (maralixibat) is the first and only approved treatment for cholestatic pruritus in patients with Alagille syndrome.
Livtencity™ is the first and only treatment for post-transplant cytomegalovirus infection in adult and paediatric patients.
Lixisenatide is an investigational glucagon-like peptide (GLP)-1 agonist being developed for the treatment of type 2 d
LODOCO® (colchicine) is the first FDA-approved anti-inflammatory atheroprotective cardiovascular treatment.
Lodotra was developed utilising SkyePharma's proprietary GeoClock and GeoMatrix technologies, for which Horizon Pharma holds an exclusive worldwide license for the delivery of corticosteroids.
Lokelma is an oral suspension of sodium zirconium cyclosilicate that is indicated for the treatment of patients with hyperkalaemia.
Lonsurf is approved for the treatment of patients with advanced metastatic colorectal cancer (mCRC).
Loqtorzi is the first and only treatment approved by the FDA for the first-line treatment of nasopharyngeal carcinoma.
Lorbrena® (lorlatinib) is an anaplastic lymphoma kinase (ALK) inhibitor indicated as a second or third-line treatment of advanced non-small cell lung cancer (NSCLC). The drug was discovered and developed by Pfizer.
Lorcaserin hydrochloride (Lorcaserin) is an investigative oral treatment drug for obesity, and was discovered by Arena P
Lovenox (enoxaparin sodium) is an anti-thrombotic drug indicated for the treatment of deep vein thrombosis (DVT) and acute ST-segment elevation myocardial infarction (STEMI).
Lucemyra™ (lofexidine) is a non-opioid medication indicated for the mitigation of opioid withdrawal symptoms.
Lucentis (ranibizumab) is a monoclonal antibody indicated for the treatment of diabetic macular edema (DME). The drug is developed by Genentech, a subsidiary of Roche Group.
LUMAKRAS (sotorasib) is approved in the US, United Arab Emirates (UAE), Canada and the UK.
Lumoxiti (Moxetumomab pasudotox) is an investigational anti-CD22 recombinant immunotoxin developed as a potential treatment for relapsed/refractory hairy cell leukaemia (HCL) patients previously treated with at least two lines of therapy.
LUPKYNIS™ (voclosporin) is a calcineurin-inhibitor immunosuppressant indicated for the treatment of adult patients with active lupus nephritis (LN).
Lurasidone is an atypical antipsychotic agent developed by Japan's Dainippon Sumitomo Pharma (DSP). The drug is indicat
Lutathera® (lutetium Lu 177 dotatate) is a peptide receptor radionuclide therapy (PRRT) indicated for the treatment of somatostatin receptor positive gastroenteropancreatic neuroendocrine tumours.
LuxturnaTM (voretigene neparvovec) is approved for the treatment of patients with biallelic RPE65 mutation-associated retinal dystrophy.
Under development by Eli Lilly, LY2140023 is a novel investigational agent for the treatment of schizophrenia. A member
Lybalvi® is a prescription medicine indicated for the treatment of adults with schizophrenia and bipolar I disorder.
Lynparza (olaparib), discovered and developed by AstraZeneca, is the first PARP inhibitor drug approved for germline BRCA-mutated advanced ovarian cancer.
Lyrica is a 3-substituted analogue of gamma-aminobutyric acid indicated to treat neuropathic pain.
Lyumjev™ (insulin lispro-aabc) is rapid-acting insulin indicated to enhance glucose control in adults with type 1 and type 2 diabetes.
Morphine-6-Glucuronide (M6G) is a new morphine derivative under development by biopharmaceutical company PAION. Developm
Discovered and developed by researchers at Pfizer, maraviroc is a novel treatment for infection due to the human immunod
Mavenclad™ (cladribine tablets) is a selective immune reconstitution therapy indicated for the treatment of active relapsing multiple sclerosis.
MAVYRET™ (glecaprevir/pibrentasvir) was developed by US-based biopharmaceutical company AbbVie as a pan-genotypic treatment for adults suffering from chronic hepatitis C virus (HCV) infection across six major genotypes (GT1 to GT6).
The drug has been approved by governmental health departments in the US, Japan, Europe, and Canada.
Mekinist (trametinib) is a mitogen-activated protein kinase (MEK) inhibitor indicated for the treatment of unresectable or metastatic melanoma in adult patients.
Menactra vaccine is developed and manufactured by Sanofi Pasteur, the vaccines division of the Sanofi Aventis Group. The
Menveo is an active immunisation vaccine indicated for the prevention of invasive meningococcal disease caused by sero
Under development by Merck & Co, Isentress (raltegravir) is an experimental drug indicated for the treatment of human im
Mirapex is indicated to treat Parkinson’s disease (PD) symptoms and restless legs syndrome (RLS).
Monovisc (sodium hyaluronate), indicated for the treatment of Osteoarthritis (OA) of the knee, is the first US Food and Drug Administration (FDA) approved single injection made with hyaluronate from a non-animal source.
MOR103 is a fully human antibody indicated for the treatment of rheumatoid arthritis (RA). The drug is being developed
Developed by MedImmune (now wholly owned by AstraZeneca), motavizumab is an investigational monoclonal antibody (MAb) in
Mounjaro™ (tirzepatide) is a first-in-class GIP and GLP-1 receptor agonist for treating type 2 diabetes.
Movantik™ (naloxegol) is an opioid antagonist therapy indicated for the treatment of opioid-induced constipation in adult patients with chronic, non-cancerous pain.
Multaq (dronedarone) is a Class III antiarrhythmic drug developed by Sanofi-Aventis (formerly Sanofi-Synthlelabo) for th
Myalepta® (metreleptin) is a recombinant human leptin analogue indicated to treat complications of congenital or acquired generalised lipodystrophy.
Mydayis is a CNS stimulant drug indicated for the treatment of attention deficit hyperactivity disorder (ADHD) in patients aged 13 years and above.
The product of a joint development programme between IVAX Corporation and Serono, Mylinax, a proprietary oral formulatio
Myobloc® (rimabotulinumtoxinB) is the first neurotoxin approved for the treatment of chronic sialorrhea in adults.
Myrbetriq (mirabegron) is a beta-3 adrenergic agonist indicated for the treatment of the overactive bladder (OAB) condition. It was developed by Japan's Astellas Pharma.
Namzaric (memantine/donepezil) is the first fixed-dose combination drug approved for the treatment of moderate and severe Alzheimer's disease in the US.
Developed by French pharmaceutical company NicOx, naproxcinod (HCT 3012) is the first in a new class of analgesic and an
Natesto (testosterone, formerly known as CompleoTRT) is the only FDA-approved nasal gel for treatment of adult males with conditions associated with deficiency or absence of endogenous testosterone.
Natpara® (parathyroid hormone), a subcutaneous injection indicated for the treatment of hypoparathyroidism, was discovered and developed by NPS Pharmaceuticals that was acquired by Shire in February 2015.
Nerlynx™ (neratinib) is a tyrosine kinase inhibitor indicated for the treatment of adult patients with early stage HER2-overexpressed or amplified breast cancer.
Nesina (alogliptin) is a dipeptidyl peptidase-4 (DPP-4) inhibitor developed and marketed by Takeda Pharmaceuticals for the treatment of diabetes 2 mellitus.
Nexavar is an oral anti-cancer agent that blocks cell proliferation and tumour angiogenesis. Developed by Bayer Healthcare with Onyx Pharmaceuticals, the drug obstructs the receptor tyrosine kinases – vascular endothelial growth factor receptor (VEGFR) VEGFR-2, VEGFR-3, platelet-derived growth factor receptor (PDGFR B), KIT, fms-related tyrosine kinase 3 (FLT-3) and RET – along the signalling pathways.
Nexium I.V. (intravenous) / esomeprazole sodium is a proton pump inhibitor manufactured and marketed by Astra Zeneca fo
NEXLETOL® (bempedoic acid) and its combination with ezetimibe NEXLIZET® are oral non-statin cholesterol-lowering drugs.
Nexviazyme® (avalglucosidase alfa-ngpt) is a new therapeutic option approved for the treatment of late-onset Pompe disease.
Under development by specialist pharmaceutical company, Neurogen, NG2-73 is a new, selective gamma-amino butyric acid (G
NGENLA® (somatrogon) is a human growth hormone analogue to treat growth failure in children aged three years and older.
NicVAX is an investigational vaccine developed for use as an aid to treat smoking addiction and prevent smoking relaps
NIKTIMVO received US FDA approval in August 2024 to treat GvHD.
Ninlaro (ixazomib) is a proteasome inhibitor indicated for the treatment of multiple myeloma.
Northera (droxidopa) is the world’s first approved therapy for symptomatic neurogenic orthostatic hypotension (NOH).
NOURIANZ (istradefylline) is indicated as adjunctive therapy to levodopa and carbidopa medications in adult patients with Parkinson’s disease (PD) to treat “off” episodes, caused when existing medications are ineffective and lead to an increase in PD symptoms.
Novavax's trivalent seasonal influenza virus-like particle (VLP) vaccine was developed to address the need to produce va
Noxafil (posaconazole) is a triazole antifungal agent indicated for treatment of the prophylaxis of invasive Aspergillus and Candida infections.
Nucala® (mepolizumab) is the first biologic therapy indicated for the treatment of hypereosinophilic syndrome (HES) in adult and paediatric patients aged 12 years and older.
Nuedexta (dextromethorphan hydrobromide / quinidine sulfate) is a combination drug indicated for the treatment of pseudobulbar affect (PBA). The drug was developed and manufactured by Avanir Pharmaceuticals.
Nulibry™ (fosdenopterin) is the first and only US Food and Drug Administration (FDA) approved treatment indicated to reduce the risk of mortality in patients with molybdenum cofactor deficiency (MoCD) Type A.
Nulojix (Belatacept) was developed by Bristol Myers Squibb and is indicated to prevent the rejection of the organ in p
Nuplazid (pimavanserin) is an atypical antipsychotic drug indicated for the treatment of Parkinson’s disease psychosis (PDP).
NURTEC® ODT (rimegepant) is the first migraine medication indicated for both acute and preventive treatment in adults.
Nuwiq injection is the first recombinant anti-haemophilic factor (blood coagulation factor VIII) drug indicated for the treatment of patients with haemophilia A.
Nymalize (nimodipine) is an oral liquid form capsule indicated to improve neurological outcomes in patients suffering from subarachnoid haemorrhage (SAH).
Obizur antihemophilic factor (recombinant) is the first recombinant porcine FVIII indicated for the treatment of bleeding episodes in adults with acquired haemophilia A (AHA).
Developed by Genentech, Ocrevus (ocrelizumab) is indicated for the treatment of relapsing multiple sclerosis (MS) and primary progressive MS.
Odomzo® (sonidegib) is an oral, selective smoothened (SMO) inhibitor indicated for the treatment of adult patients with locally advanced basal cell carcinoma (laBCC). The drug was discovered and developed by Novartis.
Discovered and developed by German pharmaceutical company Boehringer Ingelheim, Ofev (nintedanib) is the first and only tyrosine kinase inhibitor (TKI) to receive approval for the treatment of idiopathic pulmonary fibrosis (IPF).
The Phase III DeFi clinical trial for Ogsiveo demonstrated both clinically meaningful and statistically significant improvements.
Ohtuvayre™ (ensifentrine) is a novel, inhaled treatment for adult patients with chronic obstructive pulmonary disease (COPD).
OJEMDA™ (tovorafenib) is the first and only FDA-approved medicine for children with BRAF fusions or rearrangements.
Boehringer Ingelheim Pharmaceuticals’ olcegepant (BIBN 4096) is a selective Calcitonin Gene-Related Peptide (CGRP)
OLINVYK™ (oliceridine) is a new chemical agent indicated for the treatment of acute pain in adults for whom the available treatments are ineffective.
Olumiant® (baricitinib) is one of the first once-daily oral selective JAK1 and JAK2 inhibitors for the treatment of moderate-to-severe active rheumatoid arthritis (RA).
Olysio (simeprevir) is an antiviral drug indicated for the treatment of chronic hepatitis C (CHC) infection.
Omidria (ketorolac and phenylephrine/ OMS302) is the only approved drug for intraocular use to prevent intraoperative miosis and reduce postoperative pain in cataract surgery and other intraocular lens replacement (ILR) procedures.
Omontys (peginesatide) is an erythropoiesis-stimulating agent (ESA) developed for the treatment of anaemia associated with chronic kidney disease (CKD).
Omvoh™ is a biologic treatment approved for moderate to severe active ulcerative colitis (UC) in adults.
Onbrez capsules are hard capsules developed by Novartis for the treatment of chronic obstructive pulmonary disease (CO
Onfi (clobazam) is an antiepileptic drug approved to treat seizures that are associated with Lennox-Gastaut syndrome (LGS) in patients who are aged two years and above.
ONGENTYS® (opicapone) is the first and only approved catechol-O-methyltransferase (COMT) inhibitor indicated for the treatment of Parkinson's disease with off episodes, used as an adjunctive treatment to levodopa and carbidopa.
Onivyde (MM-398 / irinotecan liposome injection) is an intravenous injection indicated for the treatment of metastatic pancreatic cancer.
Onpattro™ (patisaran) is the first-of-its-kind RNA interference (RNAi)-based drug indicated for the treatment of polyneuropathy of hereditary transthyretin-mediated (hATTR) amyloidosis in adults.
ONUREG® (azacitidine) is the first and only US Food and Drug Administration (FDA)-approved drug indicated for the continued treatment of acute myeloid leukaemia (AML) in adult patients.
ONZETRA Xsail is a Food and Drug Administration (FDA)-approved intranasal dry powder formulation developed by Avanir Pharmaceuticals.
Opdivo (nivolumab) is indicated for the treatment of unresectable or metastatic melanoma in patients with a positive BRAF V600 mutation who were previously treated and made progression with Yervoy (ipilimumab).
Opdualag™ (nivolumab and relatlimab-rmbw) is indicated for the treatment of unresectable or metastatic melanoma.
Opsumit (macitentan) is an oral dual endothelin receptor antagonist indicated for the treatment of pulmonary arterial hypertension (PAH).
Opzelura (ruxolitinib) is the first and only topical treatment for repigmentation in vitiligo patients to have been approved by the Food and Drug Administration (FDA).
Oral-Lyn is an oral spray formulation of human insulin indicated for the treatment of type 1 and 2 diabetes. It is being
Orbactiv (oritavancin) is the first and only approved antibiotic for the treatment of acute bacterial skin and skin structure infections (ABSSSI) caused by susceptible Gram-positive bacteria.
Orenitram (treprostinil/UT-15C) is indicated for the treatment of pulmonary arterial hypertension (PAH), in World Health Organisation (WHO) Group I patients, to improve exercise capacity.
ORGOVYX™ (relugolix) is the first and only oral gonadotropin-releasing hormone (GnRH) receptor antagonist indicated for the treatment of advanced prostate cancer in adult patients.
ORILISSA (elagolix) is an oral gonadotropin-releasing hormone (GnRH) antagonist indicated for the treatment of moderate-to-severe pain associated with endometriosis.
Oritavancin is an investigational glycopeptide antibiotic being developed by Targanta Therapeutics for the treatment of
Orkambi (lumacaftor/ivacaftor) is the first approved medicine to treat the underlying cause of cystic fibrosis (CF), a rare, life-threatening genetic disease.
ORLADEYO™ (berotralstat) is the first oral, once-daily preventive therapy indicated for hereditary angioedema (HAE).
Orserdu™ is the first endocrine therapy for ESR1-mutated advanced or metastatic breast cancer in more than two decades.
Developed by Sanofi-Aventis (formerly Sanofi-Synthelabo), osanetant (SR-142801) is an NK3 receptor antagonist which was
Otezla (apremilast), developed by Celgene Corporation, is an inflammatory drug indicated for the treatment of adult patients with active psoriatic arthritis (PsA).
Oxbryta™ (voxelotor), previously known as GBT440, is the first and only FDA-approved sickle haemoglobin polymerisation inhibitor indicated for the treatment of sickle cell disease (SCD).
Oxervate™ (cenegermin-bkbj) is an ophthalmic solution indicated for the treatment of moderate-to-severe neurotrophic keratitis.
OXLUMO™ (lumasiran) is the first small interfering ribonucleic acid (RNAi) therapeutics indicated for the treatment of primary hyperoxaluria type 1 (PH1) to reduce urinary oxalate levels in paediatric and adult patients.
Oxtellar XR (oxcarbazepine/ SPN-804) is an anti-epileptic drug indicated for the treatment of partial seizures. The drug is developed, manufactured and marketed by Supernus Pharmaceuticals.
Oxytrol (oxybutynin) is a transdermal patch indicated for the treatment of overactive bladder in women who have symptoms of urge urinary incontinence, urgency and frequency.
Ozempic® (semaglutide) is a glucagon-like peptide (GLP-1) receptor agonist indicated for the treatment of Type 2 diabetes in adults.
Padcev (enfortumab vedotin) is the first Nectin-4-directed antibody-drug conjugate approved to treat urothelial cancer.
Palynziq™ (pegvaliase-pqpz) is a subcutaneous infusion indicated for the treatment of adults with phenylketonuria (PKU).
Pandemrix is an adjuvanted vaccine used in the prevention of the H1N1 (swine flu) virus infection and has been developed
Developed by Sinovec Biotech to provide protection against the H1N1 virus, also known as swine flu, Panflu.1 is a single
Parsabiv™ (etelcalcetide) is an intravenous injectable calcimimetic agent developed by Amgen for the treatment of secondary hyperparathyroidism (SHPT) in patients with chronic kidney disease (CKD) that were previously treated with haemodialysis.
Paxil (paroxetine hydrochloride) was first developed in 1975 by a Danish company called Ferrosan. During 1980 Ferrosan s
Paxlovid is the first FDA-approved oral antiviral treatment for mild to moderate Covid-19 in adult and paediatric patients.
Pemazyre™ (pemigatinib) is the first and only US Food and Drug Administration (FDA)-approved kinase inhibitor indicated for the treatment of cholangiocarcinoma.
PENBRAYA™ is the first pentavalent vaccine to protect adolescents against the most common types of meningococcal disease.
PEPAXTO® (melphalan flufenamide) is a first-in-class peptide-drug conjugate indicated in combination with the glucocorticoid dexamethasone for the treatment of relapsed or refractory (r/r) multiple myeloma in adult patients.
Roche / Genentech's Perjeta (Pertuzumab) is a humanised monoclonal antibody (MAb) to the HER2 receptor for the treatment of advanced breast cancer.
Axonyx, a US biopharmaceutical company that focuses on treatments for dementia, developed phenserine as a next-generatio
The formulation of Phesgo incorporates Halozyme Therapeutics’ Enhanze drug delivery technology.
PiaSky® (crovalimab), discovered by Chugai, treats paroxysmal nocturnal haemoglobinuria (PNH) in adult and paediatric patients.
Pifeltro (doravirine) is indicated for the treatment of adult patients with Human Immunodeficiency Virus-1 (HIV-1) infection.
Piqray® (alpelisib) is a kinase inhibitor indicated for the treatment of hormone receptor (HR) positive or HER2-negative advanced breast cancer with PIK3CA mutation in men and post-menopausal women.
Pirfenidone is a drug indicated for the treatment of Idiopathic Pulmonary Fibrosis (IPF), a disease that causes scarring and thickening of lungs.
Plavix (clopidogrel bisulfate) is a thienopyridine class inhibitor indicated for the treatment of acute coronary syndrome (ACS).
Under development by Novozymes A/S, the Danish biotechnology company, plectasin NZ2114 is a novel antimicrobial peptide.
Plegridy (peginterferon beta-1a) is the only pegylated beta interferon approved for the treatment of relapsing multiple sclerosis (RMS). The drug was discovered and developed by Biogen Idec.
Pluvicto™ is the first FDA-approved targeted radioligand therapy for PSMA+ metastatic, castration-resistant prostate cancer.
Polivy™ (polatuzumab vedotin-piiq) is an antibody-drug conjugate indicated for the third-line treatment of adults with relapsed or refractory (r/r) diffuse large B-cell lymphoma (DLBCL).
Pomalyst (pomalidomide) is an anti-angiogenic drug developed by Celgene Corporation for the treatment of multiple myeloma in patients who have received two prior therapies.
PONVORY™ (ponesimod) is an oral disease-modifying therapy approved for the treatment of adult patients with relapsing forms of multiple sclerosis (MS).
Portrazza (necitumumab) is a recombinant human lgG1 monoclonal antibody developed by Eli Lilly, for the treatment of metastatic squamous non-small cell lung cancer (NSCLC).
POSLUMA® is the first FDA-approved radio-hybrid PSMA-targeted agent for PET imaging of prostate cancer in adults.
Poteligeo® (mogamulizumab-kpkc) is a monoclonal antibody (mAb) indicated for the treatment of mycosis fungoides and Sézary syndrome in adults.
Pradaxa (dabigatran etexilate) is an oral anticoagulant under development by Boehringer Ingelheim. Its primary indicatio
Praluent (alirocumab) is an investigational therapy injection intended for the treatment of patients with hypercholesterolemia.
Originally discovered by Sankyo and Ube Industries, prasugrel is now the product of a co-development programme between D
Prexige (lumiracoxib) is an innovative COX-2 inhibitor developed by Novartis for the relief of pain and inflammation ass
Prezcobix™ (darunavir / cobicistat), discovered and developed by Janssen Therapeutics, is a fixed-dose antiretroviral combination tablet indicated for the treatment of human immunodeficiency virus (HIV-1) infection.
The PRIORIX vaccine is approved for the prevention of measles, mumps and rubella (MMR) in people aged 12 months and older.
Procysbi (cysteamine bitartrate) is a delayed-release capsule indicated for the treatment of nephropathic cystinosis. The drug was discovered and developed by Raptor Pharmaceutical (Raptor).
Amgen's prolia (denosumab) is a biological therapy developed for the prevention and treatment of osteoporosis and other
Promacta (eltrombopag) is the first-in-class treatment indicated for patients with severe aplastic anaemia (SAA) immunosuppressive therapy (IST) was proven ineffective for.
Provenge (sipuleucel-T) is an autologous cellular immunotherapy used intravenously in the form of infusion for the treatment of men with advanced prostate cancer.
PSI-7977 is indicated for the treatment of chronic Hepatitis C-virus (HCV) infection. The investigational drug is being
QALSODY® (tofersen) is the first therapy approved for a rare, genetic form of amyotrophic lateral sclerosis (ALS).
QINLOCK™ (ripretinib) is indicated as a fourth-line treatment for advanced gastrointestinal stromal tumour (GIST) in adult patients who have completed previous treatment with three or more kinase inhibitors, including imatinib.
Qtern (dapagliflozin and saxagliptin) is a combination drug with sodium/glucose cotransporter (SGLT) 2 and dipeptidyl peptidase 4 (DPP-4) inhibitors indicated for the treatment of type 2 diabetes.
Quillivant XR (methylphenidate) is a psychostimulant drug indicated for Attention Deficit Hyperactivity Disorder (ADHD).
Quizartinib is an investigational oral selective FLT3 inhibitor being developed for the treatment of adult patients with acute myeloid leukaemia (AML) having FLT3 internal tandem duplication (ITD) mutation.
QUVIVIQ™ (daridorexant) is a new treatment option developed by Idorsia Pharmaceuticals for adult patients with insomnia.
Afinitor (everolimus), formerly known as RAD001, is a macrolide antibiotic derived from rapamycin that is being investig
Radicava™ (edaravone) is a neuroprotective agent indicated for the treatment of amyotrophic lateral sclerosis (ALS).
Rapamune (sirolimus), an immunosuppressive agent, is the first approved medicine in the US for the treatment of lymphangioleiomyomatosis (LAM), a rare, progressive lung disease that affects the lungs, kidneys and the lymphatic system.
Rapiacta (peramivir) as is a neuraminidase inhibitor discovered and developed by BioCryst Pharmaceuticals for the treatm
Azilect® (rasagiline) is a monoamine oxidase type B (MAO-B) inhibitor indicated for the treatment of Parkinson's disease (PD).
The product of a joint development programme between Swiss companies Speedel and Novartis, Rasilez (aliskiren) is an ora
Ravicti (glycerol phenylbutyrate) is indicated for the treatment of Urea Cycle Disorders (UCD) in adults and paediatric patients aged two and above.
REBLOZYL is a first-in-class treatment for patients affected by conditions influenced by anaemia.
REGEN-COV™ (casirivimab with imdevimab) is an investigational monoclonal antibody cocktail authorised for the treatment of mild to moderate Covid-19 in adults and paediatric patients aged 12 years and older who are infected with SARS-COV-2 and are at high risk of progression to severe Covid-19.
Relyvrio is an oral, fixed-dose combination therapy for amyotrophic lateral sclerosis (ALS) in adults.
Rember (methylthioninium chloride) is a potential disease-modifying therapy for Alzheimer's disease that is under develo
Remdesivir is an investigational antiviral drug being developed by Gilead Sciences for the treatment of COVID-19, a coronavirus disease, and Ebola virus infection.
The FDA approved Repatha in December 2017 to help prevent heart attacks, strokes, and coronary revascularisations.
Restanza (cethromycin) is a second-generation ketolide, once-a-day oral antibiotic that is under review for approval by
Retevmo™ (selpercatinib) is the first therapy approved for the treatment of three rearranged during transfection (RET)-driven cancer indications.
Revatio is an approved formulation developed by Pfizer for the treatment of pulmonary arterial hypertension. The drug w
Revcovi (elapegademase-lvlr) is a PEGylated recombinant adenosine deaminase (rADA) enzyme indicated for the treatment of adenosine deaminase severe combined immune deficiency (ADA-SCID) in paediatric and adult patients.
Revlimid (lenalidomide) oral capsules are indicated for the treatment of Mantle Cell Lymphoma (MCL).
Rexulti (brexpiprazole) is a newly-discovered psychotropic compound indicated as an add-on therapy for major depressive disorder (MDD) and as a treatment for schizophrenia.
Rezdiffra is the first FDA-approved medication to treat NASH.
Developed by AGI Therapeutics, Rezular (arverapamil) is an orally administered triple-action intestinal regulator indica
REZUROCK™ (belumosudil) is an oral kinase inhibitor indicated for the treatment of chronic graft-versus-host disease (cGVHD) in patients aged 12 years and older who have received at least two failed previous lines of alternative systemic therapy.
CSL Behring's RiaSTAP is a lyophilised fibrinogen concentrate targeted at the treatment of congenital fibrinogen deficiency (CFD). It can also be used for the treatment of afibrinogenemia and hypofibrinogenemia.
Rifapentine is an antibiotic drug developed by Sanofi-aventis for treating tuberculosis (TB). It is marketed under the
Rinvoq is approved in the US and Europe for active Crohn’s disease.
Rituxan was developed by Biogen Idec, a biotechnology company based in the US, together with the copromotion partner Genentech.
Rixubis [coagulation factor IX (recombinant)] is indicated for the control and prevention of bleeding episodes and perioperative management in the treatment of adult patients suffering from haemophilia B.
Rozlytrek (entrectinib) is a kinase inhibitor indicated for the treatment of neurotrophic tyrosine receptor kinase (NTRK) fusion-positive, advanced solid tumours in adult and paediatric patients.
Poly adenosine diphosphate ribose polymerase (PARP) inhibitor Rubraca® (rucaparib) is indicated for the treatment of breast cancer susceptibility gene (BRCA) mutation-linked advanced ovarian cancer.
Ruconest (C1 Esterase Inhibitor [Recombinant]) is a recombinant approved for treatment of acute angioedema attacks in patients suffering from hereditary angioedema (HAE).
Rukobia (fostemsavir) is an antiretroviral drug, developed by ViiV Healthcare, for the treatment of HIV-1 infection in adult patients.
Agouron Pharmaceuticals, a subsidiary of Pfizer, has pioneered the development of rupintrivir (AG7088), an experimental treatment for the common cold.
Ruzurgi® (amifampridine) is approved for the treatment of Lambert-Eaton myasthenic syndrome (LEMS) in paediatric patients.
Rybelsus® (semaglutide) is the first oral glucagon-like peptide-1 (GLP-1) receptor agonist approved for the treatment of type 2 diabetes in adult patients.
Rybrevant (amivantamab-vmjw) is the first fully-human bispecific antibody indicated for the treatment of adult patients with metastatic non-small cell lung cancer (NSCLC) with epidermal growth factor receptor (EGFR) exon 20 insertion mutations, whose disease has advanced on or after platinum-based chemotherapy.
Rydapt® (midostaurin) is a multi-targeted inhibitor of multiple kinases including FMS-like tyrosine kinase 3 mutation-positive (FLT3+) and KIT approved for the treatment of acute myeloid leukaemia (AML) and three types of advanced systemic mastocytosis (SM) indications.
Rylaze (asparaginase erwinia chrysanthemi (recombinant) rywn), formerly known as JZP458, is an asparagine-specific enzyme approved for the treatment of acute lymphoblastic leukaemia (ALL) and lymphoblastic lymphoma (LBL) in certain adult and paediatric patients.
RYSTIGGO® is the first FDA-approved therapy for generalised myasthenia gravis with anti-AChR or anti-MuSK positive antibody.
The vial is available in 47mg and 188mg dosage strengths.
Sabril (vigabatrin) is an antiepileptic drug indicated for the treatment of refractory complex partial seizures (CPS) and infantile spasms (IS). It was developed by Ovation Pharmaceuticals, which was later acquired by Lundbeck.
Saphnelo is the only novel therapy approved for systemic lupus erythematosus (SLE) in more than a decade.
Sarclisa® is the first approved anti-CD38 therapy along with standard-of-care treatment to treat newly diagnosed multiple myeloma.
Sativex®, also known as Nabiximols, is indicated to treat spasticity due to multiple sclerosis and cancer pain.
The product of a joint development programme between AstraZeneca and Bristol-Myers Squibb, saxagliptin is a member of a
Saxenda is a GLP-1 receptor agonist to treat obesity in adolescents with a 60kg body weight and an initial BMI of 30kg/m².
Scemblix (asciminib) is a first-in-class STAMP inhibitor indicated for treating chronic myeloid leukaemia (CML) in adult patients.
Secuado® (asenapine) is an atypical anti-psychotic drug approved for the treatment of schizophrenia in adult patients. It is the first drug approved as transdermal patch formulation for schizophrenia treatment in the US.
Selincro (nalmefene) is an injected drug for the treatment of alcohol dependence.
Semagacestat (LY-450139) was a gamma secretase inhibitor being developed as a treatment for Alzheimer's disease by Eli
Seroquel (quetiapine fumarate) is an anti-psychotic drug indicated as an add-on treatment for patients suffering from
SF1126 is indicated for treating chronic lymphocytic leukaemia (CLL). The drug is being developed by US-based Semafore
Shingrix is a recombinant subunit shingles vaccine that was discovered and developed by GlaxoSmithKline (GSK).
Signifor (SOM230 / Pasireotide) is a somatostatin analogue indicated for the treatment of patients with Cushing's disease for whom surgery has failed. The drug is developed and manufactured by Novartis.
Siklos® is an orally administered tablet form of hydroxyurea that is indicated for the treatment of sickle-cell anaemia in paediatric patients aged two years and older.
Silenor (doxepin) is a tricyclic antidepressant indicated for the treatment of insomnia. It was developed by Somaxon Pharmaceuticals.
In March 2010, the US Food and Drug Administration (FDA) approved Silenor for the treatment of insomnia characterised by difficulty with sleep maintenance.
Simbrinza (brinzolamide/brimonidine tartrate) is a carbonic anhydrase inhibitor developed by Alcon, a division of Novartis.
Simponi (golimumab) is a subcutaneous injection for the treatment of adult patients living with ulcerative colitis (UC). The drug was discovered and developed by Janssen Biotech.
SIMPONI ARIA® (golimumab) is a fully human anti-tumour necrosis factor (TNF) alpha monoclonal antibody.
Sirturo (bedaquiline) was developed by Janssen Therapeutics, a division of Janssen Products. It is indicated for the treatment of multi-drug resistant tuberculosis (MDR-TB).
Sitavig (acyclovir) is a muco-adhesive buccal tablet indicated for the treatment of recurring Herpes Labialis. The drug is manufactured and marketed by BioAlliance Pharma.
Sivextro (tedizolid phosphate) is an oxazolidinone class antibacterial drug indicated for treatment of adult patients infected with acute bacterial skin and skin structure infections (ABSSSI) caused by susceptible gram-positive bacteria.
Skyrizi® is an interleukin-23 inhibitor indicated to treat plaque psoriasis, active psoriatic arthritis and Crohn’s disease.
Sohonos, developed by Ipsen, is the first and only approved treatment for patients with fibrodysplasia ossificans progressiva.
Developed by Sanofi, Soliqua 100/33 (insulin glargine & Lixisenatide injection) is indicated for the treatment of Type 2 diabetes.
Soliris® (eculizumab) is the first targeted therapy approved for paediatric patients with gMG in Europe.
Solithera (solithromycin) is a next-generation macrolide antibiotic developed by Cempra as a treatment for community-acquired bacterial pneumonia.
Solosec® (secnidazole) is a next-generation antibiotic indicated for the treatment of bacterial vaginosis and trichomoniasis.
Sotagliflozin is a once-daily oral drug indicated to reduce the risk of cardiovascular death in adults.
Sotyktu (deucravacitinib) is the first oral TYK2 inhibitor approved for the treatment of moderate-to-severe plaque psoriasis.
Sovaldi (sofosbuvir), developed by Gilead Sciences (Gilead), is an oral nucleotide analog inhibitor indicated for the treatment of chronic hepatitis C (CHC) infection.
Spevigo (spesolimab-sbzo) is the first approved treatment for generalised pustular psoriasis flares in adults.
SPINRAZA is available as a clear, colourless solution of 12mg/5ml dosage strength.
Spiriva is an anticholinergic drug targeted at chronic obstructive pulmonary disease (COPD). It contains tiotropium bromide as the active ingredient.
Spritam (levetiracetam) is an adjunctive therapy indicated for the treatment of seizures in patients with epilepsy, the fourth most common neurological disorder affecting people of all age groups.
Steglatro™ (ertugliflozin) is a combination drug indicated for the improvement of glycaemic control in adult patients with Type 2 diabetes mellitus.
Stelara was approved for the treatment of US adult patients with moderately to severely active UC in 2019 by the FDA.
Stimufend® (pegfilgrastim-fpgk) is a biosimilar to Neulasta® for use in patients at risk for febrile neutropenia.
Stimuvax, formerly known as BLP25 liposome vaccine (L-BLP25), is an investigational therapeutic vaccine being developed to provide immunity against the cancer cells that over express Mucin 1 (MUC-1), a glycoprotein antigen
Stiolto Respimat (tiotropium bromide and olodaterol), an oral inhalation spray indicated for the treatment of chronic obstructive pulmonary disease (COPD), is manufactured by Boehringer Ingelheim Pharmaceuticals, the US subsidiary of Boehringer Ingelheim Corp.
Stivarga (Regorafenib) is an oral multikinase inhibitor developed by Bayer HealthCare for the treatment of metastatic colorectal cancer (mCRC).
Strensiq (asfotase alfa) is the first enzyme replacement therapy (ERT) approved in the US for the treatment of perinatal / infantile and juvenile-onset hypophosphatasia (HPP), which is a life-threatening and ultra-rare metabolic disorder.
Stribild is a combination of four compounds; elvitegravir, cobicistat, emtricitabine and tenofovir disoproxil fumarate. The drug is indicated for the treatment of HIV-1 infection in adults who have never received antiretroviral treatment for the disease.
Striverdi Respimat (olodaterol) is an inhalation spray indicated for the maintenance treatment of chronic obstructive pulmonary disease (COPD), including chronic bronchitis and / or emphysema.
Sublocade™ (buprenorphine extended-release) is a partial agonist indicated for the treatment of moderate-to-severe opioid use disorder (OUD) in adults.
SUN-101 (Glycopyrrolate) is an inhalation solution developed by Sunovion Pharmaceuticals as a treatment for patients with moderate to severe chronic obstructive pulmonary disease (COPD).
Sunlenca (lenacapavir) is a first-in-class, long-acting HIV capsid inhibitor approved for the treatment of HIV-1 infection.
Surfaxin (Lucinactant) is a non-pyrogenic pulmonary surfactant used for the prevention of respiratory distress syndrome (RDS) in premature infants.
Sustiva (efavirenz) is an antiretroviral indicated for the treatment of paediatric patients with the HIV-1 infection.
Susvimo™ (ranibizumab) is a VEGF inhibitor indicated for the treatment of neovascular age-related macular degeneration (nAMD).
Sutent (sunitinib malate) is an oral multikinase inhibitor which is indicated for the treatment of progressive, well-differentiated pancreatic neuroendocrine tumours (NET).
Sycrest (asenapine) is an antipsychotic medicine indicated for the treatment of moderate to severe manic episodes associated with bipolar I disorder. The drug was developed by Merck.
Syfovre™ is the first FDA-approved treatment for geographic atrophy, an advanced form of age-related macular degeneration.
Sylvant (siltuximab) is indicated for the treatment of patients with multi-centric Castleman’s disease (MCD) in the US.
Symbicort is a combination drug comprising an inhaled corticosteroid and a long-acting bronchodilator to treat asthma.
Symdeko™ (tezacaftor/ivacaftor and ivacaftor) is a combination drug indicated for the treatment of cystic fibrosis (CF) in people aged 12 years and above.
Synribo (Omacetaxine Mepesuccinate) is a subcutaneously injected drug developed by Teva Oncology, a division of Teva Pharmaceutical Industries, based in the US. The drug is indicated for the treatment of patients with chronic myelogenous leukaemia (CML) in both chronic and accelerated phases.
T-705 is a novel oral agent indicated for the treatment of influenza that is under development by Toyama Chemical of Jap
Tabrecta™ (capmatinib) is the first US Food and Drug Administration (FDA)-approved therapy for the treatment of adult patients diagnosed with metastatic non-small cell lung cancer (NSCLC) whose tumours have a mutation that results in mesenchymal-epithelial transition (MET) exon 14 (METex14) skipping.
Tafinlar (dabrafenib) is a single-agent oral treatment indicated for the treatment of unresectable or metastatic melanoma in adult patients.
Tagrisso (osimertinib) is a once-daily tablet developed by AstraZeneca for the treatment of metastatic epidermal growth factor receptor (EGFR) T790M mutation associated with non-small cell lung cancer (NSCLC).
Takhzyro (lanadelumab-flyo) is indicated for the preventive treatment of hereditary angioedema (HAE) in patients aged 12 years and older.
Taltz® (ixekizumab) is the first humanised interleukin (IL)-17A antagonist therapy approved for the treatment of active non-radiographic axial spondyloarthritis (nr-axSpA) in adult patients with objective inflammation signs.
The US FDA granted accelerated approval to TALVEY in August 2023.
Talzenna™ (talazoparib) is an inhibitor of the poly adenosine diphosphate (ADP) ribose polymerase (PARP) enzyme that is indicated for the treatment of human epidermal growth factor receptor 2 (HER2) negative breast cancer in adult patients with the BRCA-mutated (gBRCAm) gene.
Tamiflu or oseltamivir is a prescription drug used for prophylaxis and treatment of flu caused by influenza virus types A (H1N1) and B.
Tanzeum (albiglutide), developed by GlaxoSmithKline (GSK), is a GLP-1 receptor agonist indicated for treatment of type 2 diabetes.
Taranabant is a highly selective cannabinoid-1 (CB1) receptor inverse agonist developed by Merck & Co for the treatment
Tarceva (erlotinib) is an oral anti-cancer drug developed by OSI Pharmaceuticals, Genentech and Roche. It is a member of
TARPEYO is the first and only FDA-approved therapy to reduce the loss of kidney function in adults with primary IgAN.
Tasigna (nilotinib) is indicated for treating Philadelphia chromosome positive chronic myeloid leukaemia (Ph+ CML). Th
TAVALISSE™ is a twice-daily regimen indicated for the treatment of chronic immune thrombocytopenia (ITP) in adult patients who have had an insufficient response to a previous treatment.
Tavneos (avacopan) is the first FDA-approved oral selective complement 5a receptor inhibitor drug for ANCA-associated vasculitis.
Tazverik is the first approved treatment for metastatic/locally advanced epithelioid sarcoma in patients aged 16 years and older.
The product of a co-development programme between ThromboGenics, a Belgian biotechnology company, and BioInvent Internat
TBRIA (calcitonin-salmon [rDNA origin] delayed release tablet) is the first oral recombinant salmon calcitonin, developed by Tarsa Therapeutics, for the treatment of postmenopausal osteoporosis.
Tecartus™ (brexucabtagene autoleucel, formerly KTE-X19) chimeric antigen receptor (CAR) T-cell therapy is the first and only approved cell-based gene therapy for the treatment of mantle cell lymphoma (MCL).
TECELRA® (afamitresgene autoleucel) is the first novel treatment option for individuals with synovial sarcoma in more than ten years.
Tecentriq® (atezolizumab) is a monoclonal antibody designed to bind with a protein called PD-L1.
Tecfidera (BG-12/Dimethyl Fumarate) is a first-line oral treatment indicated for patients with relapsing-remitting multiple sclerosis (RRMS). The drug was developed by Biogen Idec.
Technivie (ombitasvir, paritaprevir and ritonavir) is the first direct-acting antiviral drug approved for the treatment of genotype 4 (GT4) chronic hepatitis C virus (HCV) infection in the US.
Tegsedi™ (inotersen) is an anti-sense oligonucleotide indicated for the treatment of polyneuropathy of hereditary transthyretin-mediated (hATTR) amyloidosis in adult patients.
The product of a joint collaborative programme between Idenix Pharmaceuticals and Novartis Pharma, telbivudine (oral L-d
Tepmetko (tepotinib) is an oral kinase inhibitor approved for the treatment of patients with metastatic non-small cell lung cancer (NSCLC). It is the first and only US Food and Drug Administration (FDA) approved mesenchymal-epithelial transition (MET) inhibitor with once-daily oral dosing.
Terlivaz (terlipressin) is the first and only approved treatment of hepatorenal syndrome (HRS) in adults.
Tesmilifene is a small molecule chemopotentiator under development by YM BioSciences, a Candian pharmaceutical company t
Under development by NeuroSearch, a Danish pharmaceutical company, tesofensine is a novel treatment for obesity. A serot
Tezspire (tezepelumab-ekko) is the first and only biologic indicated as an add-on maintenance treatment for severe asthma.
TIBSOVO® (ivosidenib) is the first approved targeted therapy for patients with IDH1-mutated advanced cholangiocarcinoma.
TIGLUTIK (Riluzole) is a neuroprotective agent indicated for the treatment of amyotrophic lateral sclerosis (ALS).
Tivdak (tisotumab vedotin-tftv) is the first and only approved antibody-drug conjugate to treat adults with cervical cancer.
Tivicay (dolutegravir) is an integrase inhibitor indicated for the treatment of the HIV-1 infection in adults and children aged 12 years and above.
Tivorbex (indomethacin) is a nonsteroidal anti-inflammatory drug (NSAID) indicated for the treatment of mild to moderate acute pain in adults.
Toujeo (insulin glargine [rDNA origin]) is an insulin injection approved for the treatment of type 1 and type 2 diabetes to improve glycaemic control in adult patients.
TRA-SCH 530348 is an oral antiplatelet drug under development by Schering-Plough for the treatment and prevention of ath
Linagliptin (BI-1356), which is being marketed under the trade name Tradjenta®, is an oral dipeptidyl peptidase-4 (DPP-4) inhibitor drug for the treatment of type 2 diabetes.
Translarna™ (ataluren) is a protein restoration therapy indicated for the treatment of nonsense mutation Duchenne muscular dystrophy (nmDMD). The drug was developed by PTC Therapeutics.
Trastuzumab, indicated for the treatment of recurrent gastric cancer with a high concentration of HER2 (human epiderma
Tremfya™ (guselkumab) is a biologic approved for the treatment moderate-to-severe plaque psoriasis in adults.
Novo Nordisk’s Tresiba® (insulin degludec) is indicated for the treatment of Type 1 and Type 2 diabetes.
Tretten is the world’s first recombinant treatment available for the prevention of bleeding in adults and children suffering from congenital factor XIII (FXIII) A-subunit deficiency.
The product of a joint development programme between US drug development company Pozen and GSK, Treximet is a novel comb
TRIKAFTA is the first triple combination therapy containing elexacaftor, ivacaftor, and tezacaftor indicated for the treatment of cystic fibrosis (CF) in people aged 12 years and above and having a F508del mutation and one minimal function mutation.
Triumeq (dolutegravir/abacavir/lamivudine) is an investigational drug indicated for the treatment of adult and adolescent patients (minimum age of 12 years and with a minimum weight of 40kg) affected with Human Immunodeficiency Virus (HIV).
Trobalt (ezogabine / retigabine) is indicated for the treatment of partial-onset epileptic seizures in patients aged more than 18 years old.
Gilead’s Trodelvy is indicated for the treatment of locally advanced or metastatic breast cancer and urothelial cancer.
Daybue is the first and only drug approved for the treatment of Rett syndrome, a rare neurodevelopmental disorder.
Trogarzo™ is indicated for the treatment of multidrug-resistant HIV-1 infection in heavily treatment-experienced patients.
Trulance™ (Plecanatide) is a guanylate cyclase-C (GC-C) agonist indicated for the treatment of adult patients with chronic idiopathic constipation (CIC).
Trulicity (dulaglutide) is a glucagon-like peptide 1 receptor agonist (GLP-1 agonist) indicated for the treatment of adults with type 2 diabetes. The drug was discovered and developed by Eli Lilly and Company.
Trumenba is a vaccine licenced in the US for the prevention of invasive meningococcal meningitis B in adolescents and young adults between ten and 25 years.
TRUQAP™ (capivasertib) in combination with Faslodex® (fulvestrant) is indicated for the treatment of breast cancer in adults.
TRUSELTIQ™ (infigratinib) is an oral kinase inhibitor indicated for the treatment of previously treated, unresectable locally advanced or metastatic cholangiocarcinoma (CCA) with a fibroblast growth factor receptor II (FGFR2) fusion in adult patients.
Truvada (emtricitabine and tenofovir disoproxil fumarate) is an antiretroviral indicated for preventing or reducing the risk of acquiring HIV-1.
ruxima™ (rituximab) is the first biosimilar monoclonal antibody (mAb) approved for the treatment of haematological cancers, including diffuse large B-cell lymphoma, follicular lymphoma, chronic lymphocytic leukaemia, and rheumatoid arthritis, as well as granulomatosis with polyangiitis and microscopic polyangiitis.
Tudorza Pressair (aclidinium bromide inhalation powder) is an anticholinergic drug indicated for the long-term maintenance treatment of bronchospasm associated with chronic obstructive pulmonary disease (COPD), including chronic bronchitis and emphysema. It was developed by Forest Laboratories in collaboration with Spanish company Almirall.
TUKYSA™ (tucatinib) is the first HER-2 tyrosine kinase inhibitor approved in combination with trastuzumab and capecitabine for the treatment of HER2-positive metastatic breast cancer.
Developed by Wyeth Pharmaceuticals, Tygacil (tigecycline) is the first in a new class of antibiotics, the glycylcyclines
Tykerb (lapatinib ditosylate) is an epidermal growth factor receptor (EGFR) and ErbB-2 (Her2/neu) dual tyrosine kinase i
Tyrvaya (varenicline) is the first and only nasal spray approved by the FDA for the treatment of dry eye disease.
The product of a joint development programme between by Elan Pharmaceuticals and Biogen, Tysabri (natalizumab) is a huma
Uceris (budesonide) is glucocorticoid receptor that is indicated for the treatment of ulcerative colitis. It is developed by US-based biopharmaceutical company Santarus, in collaboration with Cosmo Technologies.
UKONIQ™ (umbralisib) is the first and only oral, dual inhibitor of phosphoinositide 3 kinase (PI3K) delta and casein kinase 1 (CK1) epsilon, indicated for the treatment of previously treated relapsed or refractory marginal zone lymphoma (MZL) and follicular lymphoma (FL) in adult patients.
Ultomiris™ (ravulizumab-cwvz) is a complement inhibitor drug approved for the treatment of paroxysmal nocturnal haemoglobinuria (PNH) in adults.
Aptalis Pharma's Ultresa is indicated for the treatment of exocrine pancreatic insufficiency (EPI) caused by cystic fibrosis or other conditions. It was approved by the US Food and Drug Administration.
Ustekinumab (CNTO 1275), a human anti-interleukin 12 (IL-12) and anti-interleukin 23 (IL-23) monoclonal antibody (MAb),
V1512 (melevodopa/carbidopa) is an effervescent tablet formulation for the treatment of Parkinson's disease.
Vabysmo™ (faricimab-svoa) is the first injectable eye medicine approved for two conditions, nAMD and DME, simultaneously.
In partnership with Novartis Pharma, Idenix Pharmaceuticals is developing valtorcitabine (L-deoxycytidine) as part of a
VANFLYTA® (quizartinib) is the first and only FLT3 inhibitor indicated to treat newly diagnosed acute myeloid leukaemia.
Varithena (Polidocanol Injectable Foam) is injectable foam indicated for the treatment of patients with incompetent veins and visible varicosities of the great saphenous vein (GSV) system.
VariZIG (Varicella Zoster Immune Globulin Human) is an antibody drug that is indicated for the post-exposure prevention of chickenpox in immunocompromised children, newborns and pregnant women. It was developed by Cangene Corporation, a Canada-based company.
Veletri (epoprostenol) is an eicosanoid indicated for controlling functions in the body such as blood pressure and muscle contractions. It was originally developed by GeneraMedix.
Velphoro (sucroferric oxyhydroxide / PA21) is an iron-based Ca-free phosphate binder for treating Hyperphosphatemia in Chronic Kidney Disease (CKD) patients on dialysis.
Developed by Gilead Sciences, Vemlidy (tenofovir alafenamide) is indicated for treatment of hepatitis B (HBV) virus infection with compensated liver disease in adult patients.
Venclexta (Venetoclax) is an oral formulation developed by AbbVie in collaboration with Genentech and Roche, for the treatment of chronic lymphocytic leukaemia patients with 17p deletion.
Veopoz received FDA approval for the treatment of PLE in August 2023.
VEOZAH™ (fezolinetant) is an FDA-approved nonhormonal treatment for vasomotor symptoms (VMS) due to menopause.
Verquvo (vericiguat) is the first soluble guanylate cyclase (sGC) stimulator approved to treat heart failure.
Verzenio (abemaciclib) is a cyclin-dependent kinases (CDK) 4 and 6 inhibitor indicated for the treatment of women with hormone receptor-positive (HR+) human epidermal growth factor receptor 2-negative (HER2-) advanced or metastatic breast cancer.
Vesicare (solifenacin succinate) is an oral selective muscarinic receptor antagonist developed by Yamanouchi, Japan's th
Viberzi (eluxadoline), an oral tablet developed by Actavis, is indicated for the treatment of adults suffering from irritable bowel syndrome with diarrhoea (IBS-D).
Viekirax (ombitasvir / paritaprevir / ritonavir) and Exviera (dasabuvir) is indicated for the treatment of genotype 1 chronic hepatitis C virus (HCV) infection and compensated cirrhosis.
Viibryd (Vilazodone) is an antidepressant manufactured for the treatment of adults with major depressive disorder (MDD). T
Novartis' Galvus (vildagliptin) is a member of a new class of oral antidiabetic agents known as dipeptidyl peptidase IV
VILTEPSO™ (viltolarsen) is an antisense oligonucleotide drug indicated to treat Duchenne muscular dystrophy (DMD), a rare genetic disorder, in patients with a confirmed DMD gene mutation that is vulnerable to exon 53 skipping therapy.
Vimizim (elosulfase alfa / BMN 110) is an enzyme replacement therapy (ERT) for treating patients with Morquio A syndrome (MPS IVA).
VIMPAT® (lacosamide) is a federally-controlled drug (CV) indicated as a supplementary therapy for the treatment of primary generalised tonic-clonic seizures (PGTCS) in patients aged four years and older.
Vitrakvi® (larotrectinib) is an oral tyrosine kinase (TRK) inhibitor indicated for the treatment of advanced solid tumours in adult and paediatric patients with neurotrophic receptor tyrosine kinase (NTRK) gene fusion.
VIVJOA is the first and only FDA-approved drug for the treatment of recurrent vulvovaginal candidiasis (RVVC) in females.
Vizimpro® (dacomitinib) is a kinase inhibitor indicated for the treatment of EGFR-positive advanced non-small cell lung cancer (NSCLC) patients diagnosed with exon 19 deletion or exon 21 L858R substitution mutations.
Volasertib (BI 6727) is a selective and potent polo-like kinase (Plk) inhibitor currently being investigated for the treatment of patients with acute myeloid leukaemia (AML).
VONJO (pacritinib) is the first oral kinase inhibitor approved for the treatment of myelofibrosis and thrombocytopaenia.
VOQUEZNA is a co-packaged medicine containing vonoprazan with antibiotics for the treatment of H pylori infection.
VORANIGO® (vorasidenib) is the first FDA-approved targeted therapy for Grade 2 isocitrate dehydrogenase (IDH)-mutant glioma.
Voraxaze (glucarpidase) is an antidote indicated for the treatment of plasma methotrexate (MTX) toxicity in patients with delayed elimination of methotrexate due to kidney dysfunction.
Voreloxin is a quinolone derivative being investigated for the treatment of various cancers. The drug is being develop
Vosaroxin is a first-in-class anticancer quinolone derivative (AQD) under development by Sunesis Pharmaceuticals for th
Vosevi™ (Sofosbuvir/Velpatasvir/Voxilaprevir) is a direct-acting antiviral (DAA) indicated for the treatment of chronic hepatitis C virus (HCV) infection in adults with genotypes one to six.
GlaxoSmithKline's (GSK's) Votrient drug is an approved medication for the treatment of renal cell cancer (RCC). The RRC treatment drug has conditional marketing authorisation in the European Union (EU).
VOWST™ is the first and only FDA-approved orally administered microbiota-based therapy to prevent the recurrence of CDI.
VOXZOGO (vosoritide) is the first approved therapeutic treatment for achondroplasia and epiphyses.
Designed for specific mood disorders, Vraylar (cariprazine) is approved for bipolar disorder, schizophrenia and major depressive disorder.
Vtama® (tapinarof) is a steroid-free, topical treatment option for mild to severe plaque psoriasis in adults.
Vuity (pilocarpine HCl) eye drop is the first-of-its-kind FDA-approved treatment for age-related blurry presbyopia in adults.
VUMERITY™ (diroximel fumarate), previously known as ALKS 8700, is a novel oral formulation indicated for the treatment of relapsing forms of multiple sclerosis (MS).
VYLOY™ (zolbetuximab) is the first and only CLDN18.2-targeted therapy approved for the treatment of gastric cancer.
Vyndaqel (tafamidis meglumine) is a first-in-class transthyretin stabiliser indicated for the treatment of Transthyretin Familial Amyloid Polyneuropathy (TTR-FAP).
Vyvanse® (lisdexamfetamine dimesylate) is a central nervous system (CNS) stimulant indicated for the treatment of moderate-to-severe binge-eating disorder and attention deficit hyperactivity disorder (ADHD).
Developed by argenx, VYVGART is approved in the US, Europe, Japan, China and Israel.
WAINUA™ (eplontersen) is the only medicine for managing transthyretin-mediated amyloid polyneuropathy (ATTRv-PN), allowing self-administration through an auto-injector.
WAKIX® (pitolisant) is the first and only non-scheduled medication indicated for the treatment of cataplexy or excessive daytime sleepiness (EDS) in adult patients with narcolepsy.
The FDA approved semaglutide under the brand name Wegovy for chronic weight management in adults in June 2021.
Wilate is a von Willebrand Factor/Coagulation Factor VIII (vWF/FVIII) concentrate developed for the treatment of von W
Winrevair (sotatercept) is a breakthrough biologic treatment for the rare and progressive pulmonary arterial hypertension (PAH).
Xadago® (safinamide) is a monoamine oxidase type B (MAO-B) inhibitor indicated for the treatment of Parkinson's disease.
The FDA approved Xalkori for the treatment of metastatic Anaplastic Lymphoma Kinase (ALK) positive non-small cell lung cancer in August 2011.
The product of a joint development programme between Bayer and Johnson & Johnson, Xarelto (rivaroxaban) is a new oral anticoagulant. It is indicated for the primary prevention and treatment of venous thromboembolism (VTE) following orthopaedic surgery. Clinical trials are also ongoing to evaluate Xarelto (rivaroxaban) for stroke prevention in patients with atrial fibrillation and acute coronary syndrome.
Xeljanz (tofacitinib) is a janus kinase (JAK) 3 inhibitor developed by Pfizer as a treatment for the symptoms of rheumatoid arthritis.
Xeljanz XR (tofacitinib citrate) is an 11mg once-daily oral JAK inhibitor developed by Pfizer for the treatment of moderate to severe Rheumatoid Arthritis (RA).
Xeloda is an approved oral drug developed by F. Hoffmann-La Roche (Roche) for treating metastatic colorectal cancer and
Xenpozyme is the first enzyme replacement therapy for acid sphingomyelinase deficiency approved in Japan and Europe.
Xgeva (denosumab) is a preventive medicine developed by Amgen to check the spread of cancer to the bones.
Xhance™ (fluticasone propionate / previously known as OPN-375), a synthetic trifluorinated corticosteroid, is indicated for the treatment of nasal polyps in patients aged 18 years or older.
Xiaflex is the first drug indicated for treating Dupuytren's contracture. The drug was developed by Auxilium Pharmaceuticals in collaboration with BioSpecifics Technologies.
Xiidra lifitegrast ophthalmic solution is a twice-a-day eye drop solution developed by Shire as a treatment for the signs and symptoms of dry eye disease in adults.
Xipere™ is the first and only FDA-approved therapy for suprachoroidal use to treat macular oedema associated with uveitis.
XL184 (cabozantinib) is an indicator to inhibit tumour growth, angiogenesis and metastasis.
Xofigo (radium 223 dichloride) is an intravenous radiotherapeutic drug indicated for the treatment of patients suffering from prostate cancer with bone metastases.
The product of a joint development programme between Tanox, Genentech and Novartis, Xolair (omalizumab) is a recombinant
XOLREMDI™ (mavorixafor) is the first approved therapy specifically indicated to treat patients with WHIM syndrome.
Xospata® (gilteritinib) is a feline McDonough sarcoma (FMS) like tyrosine kinase 3 (FLT3) inhibitor indicated for the treatment of relapsed or refractory acute myeloid leukaemia (AML) with FLT3 mutation in adult patients.
XPOVIO® (selinexor) is the only single-agent oral therapy indicated for the treatment of patients with relapsed or refractory diffuse large b-cell lymphoma (DLBCL).
Xtandi (enzalutamide) is an androgen receptor inhibitor indicated for the treatment of metastatic castration-resistant prostate cancer (mCRPC).
Developed by Novo Nordisk, Xultophy 100/3.6 is indicated for the treatment of type 2 diabetes.
Jazz Pharmaceuticals’ XYWAV™ (calcium, magnesium, potassium, and sodium oxybates) is the first US Food and Drug Administration (FDA) approved medicine indicated for the treatment of cataplexy and excessive daytime sleepiness (EDS) associated with narcolepsy in over 15 years.
Yervoy is a monoclonal antibody drug indicated for treating metastatic melanoma. The drug was developed by Bristol-Myers
Yescarta™ (axicabtagene ciloleucel) is one of the first chimeric antigen receptor T cell (CAR T) therapies indicated for the treatment of relapsed / refractory large B-cell lymphoma in adult patients.
Yupelri™ (revefenacin) is a long-acting muscarinic antagonist (LAMA) indicated as a maintenance treatment for chronic obtrusive pulmonary disease (COPD) in adult patients.
Zactima (vandetanib) is an orally available tyrosine kinase inhibitor (TKI) developed by AstraZeneca for the treatment o
Zaltrap (ziv-aflibercept) is a recombinant fusion protein indicated for the treatment of metastatic colorectal cancer (mCRC). It was developed by Sanofi-Aventis in collaboration with Regeneron Pharmaceuticals.
Zegerid is a proton pump inhibitor (PPI) comprising omeprazole, a leading prescription acid that reduces heartburn and s
Zejula™ (niraparib) is a poly adenosine diphosphate (ADP) ribose polymerase (PARP) inhibitor approved for the treatment of adult patients with ovarian cancer.
Zelboraf is indicated for the treatment of metastatic melanoma and Erdheim-Chester disease.
Zepatier is a once-daily oral medicine comprising 50mg of non-structural protein 5A (NS5A) replication complex inhibitor elbasvir and 100mg of NS3/4A protease inhibitor grazoprevir.
ZEPOSIA® (Ozanimod) is the only FDA approved sphingosine-1-phosphate (S1P) receptor modulator indicated for the treatment of relapsing forms of multiple sclerosis (RMS) in adults.
Zepzelca™ (lurbinectedin) is a prescription medicine indicated for the treatment of adult patients with metastatic small cell lung cancer (SCLC) with disease progression on or after platinum-based chemotherapy.
Zerbaxa (ceftolozane/tazobactam) is an antibiotic developed and marketed by Merck (formerly Cubist Pharmaceuticals (Cubist)), for the treatment of infections caused by gram-negative bacteria.
Zilretta™ (triamcinolone acetonide extended-release injectable suspension) is a US Food and Drug Administration (FDA) approved extended-release intra-articular therapy indicated for the treatment of osteoarthritis knee pain.
Zinbryta (daclizumab) is an injectable formulation jointly developed by Biogen and Abbive for the treatment of relapsing forms of multiple sclerosis (MS) in adults.
Zinforo (ceftaroline fosamil) is a new intravenous cephalosporin antibiotic indicated for the treatment of serious skin infections or community-acquired pneumonia.
Zinplava (bezlotoxumab) is an injectable solution developed by Merck indicated for the treatment of clostridium difficile infection (CDI) in adult patients who are already receiving anti-bacterial drug treatment.
Zioptan (tafluprost ophthalmic solution) was developed by Santen Pharmaceutical in collaboration with Merck. The drug is indicated for the reduction of elevated intraocular pressure (IOP). In February 2012, Zioptan received approval for the reduction of IOP in patients suffering from ocular hypertension or open-angle glaucoma.
Zohydro (hydrocodone) is a single-entity oral drug indicated for the treatment of chronic pain. San Diego-based pharmaceutical company Zogenix developed and commercialised the drug in the US.
Zokinvy (lonafarnib) is the first approved therapy for the group of ultra-rare genetic diseases collectively known as progeria.
Zolgensma® (onasemnogene abeparvovec-xioi) is a one-time gene therapy indicated for the treatment of spinal muscular atrophy (SMA) in paediatric patients.
Zometa is a bone resorption inhibitor indicated for the treatment of bone complications in patients with advanced cancer. It has several anticancer properties.
Zonegran (Zonisamide) is an anti-epileptic drug indicated for the treatment of partial seizures in adults with epilepsy with or without secondary generalisation.
Zontivity (vorapaxar) is a protease-activated receptor-1 (PAR-1) antagonist indicated for the reduction of thrombotic cardiovascular events in patients with a history of heart attack or peripheral arterial disease (PAD).
Zorvolex (diclofenac) is a nonsteroidal anti-inflammatory drug currently indicated for the treatment of mild to moderate acute pain in adults.
ZTALMY® is the first FDA-approved therapy for seizures due to CDLK5 deficiency disorder in patients aged two years and older.
Zubsolv (buprenorphine and naloxone) is a sublingual tablet indicated as maintenance treatment for people suffering from opioid dependence.
Zybrestat is a vascular disrupting agent (VDA) indicated for the treatment of anaplastic thyroid cancer and, potentially
Zydelig (idelalisib) is a phosphoinositide 3-kinase (PI3K) delta inhibitor and is used for the treatment of three B-cell blood cancers: relapsed chronic lymphocytic leukaemia (CLL), follicular lymphoma (FL) and small lymphocytic lymphoma (SLL).
Zykadia (Ceritinib / LDK378) is an inhibitor of anaplastic lymphoma kinase (ALK) indicated for treatment of non-small cell lung cancer (NSCLC).
Zynteglo™ is a gene therapy indicated for the treatment of transfusion-dependent beta (β)-thalassemia (TDT) in patients aged 12 years and older.
The drug holds orphan drug designation by the FDA for the treatment of anal cancer.
Zyprexa (olanzapine) belongs to a newer group of antipsychotic medications called atypical antipsychotics and is widely
Developed by Coughar Biotechnology, abiraterone acetate (CB7630) was discovered by the UK Institute for Cancer Research.