drugset / Trial / NCT03829501

A Phase 1/2, Open-label, Multi-center Study of the Safety and Efficacy of Alomfilimab (KY1044) as Single Agent and in Combination With Anti-PD-L1 (Atezolizumab) in Adult Patients With Selected Advanced Malignancies

NCT03829501

Phase 1/2 Terminated 222 enrolled Kymab Limited Sanofi · collab
Non-randomizedSequentialOpen-labelTreatment

Summary

A Phase 1/2, open label, multi-center study to evaluate the safety, efficacy and tolerability of alomfilimab as single agent and in combination with anti-PD-L1 (atezolizumab) in adult patients with selected advanced malignancies, who are ineligible for or there are no available therapies known to confer a clinical benefit for their disease, or they have exhausted all such available options in each indication and therefore will be patients for whom a clinical trial is appropriate.

Timeline

Start
2019-01-28
Primary completion
2024-10-03
Completion
2024-10-03

Drugs

EvaluationDrugModalityDoseRoute
Subject Alomfilimab Monoclonal antibody 0.8 mg Intravenous
Subject Alomfilimab Monoclonal antibody 2.4 mg Intravenous
Subject Alomfilimab Monoclonal antibody 24 mg Intravenous
Subject Alomfilimab Monoclonal antibody 80 mg Intravenous
Subject Alomfilimab Monoclonal antibody 240 mg Intravenous
Subject Atezolizumab Monoclonal antibody 1200 mg Intravenous