drugset / Trial / NCT03212404
Phase 1 Study of CK-301 (Cosibelimab) as a Single Agent in Subjects With Advanced Cancers
Phase 1
Active not recruiting
272 enrolled
Checkpoint Therapeutics, Inc.
Novotech (Australia) Pty Limited · collab
NaSingle-groupOpen-labelTreatment
Summary
CK-301 (cosibelimab) is a fully human monoclonal antibody of IgG1 subtype that directly binds to Programmed Death-Ligand 1 (PD-L1) and blocks its interactions with the Programmed Death-1 (PD-1) and B7.1 receptors. The primary objectives of this study are to assess the safety, tolerability and efficacy of CK-301 when administered intravenously as a single agent to subjects with selected recurrent or metastatic cancers.
Timeline
- Start
- 2017-09-20
- Primary completion
- 2021-11-18
- Completion
- 2025-12
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Cosibelimab | Monoclonal antibody | 800 mg | Intravenous |