drugset / Trial / NCT06418061
Study of IBI3005 in Subjects With Unresectable, Locally Advanced or Metastatic Solid Tumors
NaSequentialOpen-labelTreatment
Summary
The main purpose of this study is to evaluate the safety and tolerability of IBI3005 and to determine the maximum tolerated dose (MTD) and the recommended Phase 2 Dose (RP2D) of IBI3005.
Timeline
- Start
- 2025-01-08
- Primary completion
- 2027-06-30
- Completion
- 2027-12-31
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | IBI3005 | Monoclonal antibody | — | — |