drugset / Trial / NCT04372433
IO-202 as Monotherapy and IO-202 Plus Azacitidine ± Venetoclax in Patients in AML and CMML
Phase 1
Completed
67 enrolled
Immune-Onc Therapeutics
California Institute for Regenerative Medicine (CIRM) · collab
Non-randomizedSequentialOpen-labelTreatment
Summary
To assess safety and tolerability at increasing dose levels of IO-202 in successive cohorts of participants with AML with monocytic differentiation and CMML in order to estimate the maximum tolerated dose (MTD) or maximum administered dose (MAD) and select the recommended Phase 2 dose (RP2D)
Timeline
- Start
- 2020-09-14
- Primary completion
- 2025-01-31
- Completion
- 2025-01-31
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Azacitidine | Other / unclassified | — | Intravenous |
| Subject | IO-202 | Monoclonal antibody | — | Intravenous |
| Background | Venetoclax | Small molecule | — | — |