drugset / Trial / NCT06418061

Study of IBI3005 in Subjects With Unresectable, Locally Advanced or Metastatic Solid Tumors

NCT06418061

Phase 1 Recruiting 198 enrolled Innovent Biologics (Suzhou) Co. Ltd.
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

EvaluationDrugModalityDoseRoute
Subject IBI3005 Monoclonal antibody