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
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
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| 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 |