OSE-279 is intended for the treatment of advanced solid tumours. Credit: SciPro/Shutterstock.com.

OSE Immunotherapeutics has reported positive results from the first-in-human Phase I/II study of OSE-279 to treat advanced solid tumours.

The dose escalation and expansion study intends to determine the maximum tolerated dose (MTD) and the recommended Phase II dose (RP2D) of an anti-PD1 monoclonal antibody OSE-279.

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In this study, OSE-279 will be evaluated as a monotherapy in advanced solid tumours with two possible administration rates.

Assessing antitumour activity, safety profile, pharmacokinetic (PK) and receptor occupancy or pharmacodynamic (PD) profile of OSE-279 are the secondary objectives of the study.

Thirteen patients with eight tumour types received OSE-279 100mg and 300mg every three weeks (q3w) or 600mg every six weeks (q6w).

The data, presented at the AACR-NCI-EORTC International Conference on Molecular Targets and Cancer Therapeutics held in Boston, showed a manageable safety profile with preliminary signs of efficacy in these patients.

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One confirmed partial response was observed in hepatocellular carcinoma patients who received a single dose of OSE-279 300mg.

The study also reported two yet unconfirmed partial responses in anal squamous cell carcinoma and undifferentiated pleomorphic sarcoma patients who received OSE-279 600mg.

Furthermore, stable disease longer than 16 weeks was observed in three patients with a disease control rate of 55%.

Both PK and PD profiles were consistent with modelling and PK profile showed good exposure and dose-proportionality.

Besides, receptor occupancy was maintained and within the boundaries of the simulation.

OSE-279 blocks both PD-L1 and PD-L2, the ligands of PD1 overexpressed by tumour cells and tumour microenvironment.

The company’s pipeline also includes Tedopi, OSE-127, FR-104/VEL-101, and OSE-172/BI 765063.