drugset / Trial / NCT07335497

CR-001 in Adult Participants With Locally Advanced or Metastatic Solid Tumors

NCT07335497 ↗

Phase 1/2 Recruiting 290 enrolled Crescent Biopharma, Inc.
Non-randomizedSequentialOpen-labelTreatment

Summary

The purpose of this study is to determine the safety and tolerability of monotherapy CR-001 and identify the maximum tolerated dose (MTD), and/or optimal biologic dose and Recommended Phase 2 Dose(s) (RP2D) in participants with locally advanced or metastatic solid tumors.

Timeline

Start
2026-02-17
Primary completion
2029-02
Completion
2029-02

Drugs

EvaluationDrugModalityDoseRoute
Subject CR-001 Unknown — Intravenous

Indications

No indication recorded.