ExeVir’s Covid-19 therapy shows neutralisation against omicron variants
ExeVir’s antibody therapy, XVR012, has shown neutralisation potency with an IC50 range of 0.8-1.8 against all SARS-CoV-2 variants including E.G.5.1, HV.1 and BA.2.86.1.
16 January 2024
16 January 2024
ExeVir’s antibody therapy, XVR012, has shown neutralisation potency with an IC50 range of 0.8-1.8 against all SARS-CoV-2 variants including E.G.5.1, HV.1 and BA.2.86.1.
The INITIUM trial was conducted at 39 hospitals in the US, UK, Belgium and Norway.
The trial will assess the preliminary efficacy of the antibody NWY001 in patients with advanced solid tumours.
The dihydroartemisinin–piperaquine combination regimen was found to reduce malaria risks among pregnant women with HIV.
The trial will assess if the inhalatory method can protect against TB more effectively than the traditional intradermal injection.
Theralase plan to re-submit a pre-breakthrough therapy designation to the US Food and Drug Administration in Q1 2024.
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