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RECRUITING
NCT07909031
PHASE1/PHASE2

CR-002 in Adult Participants With Locally Advanced or Metastatic Solid Tumors

Sponsor: Crescent Biopharma, Inc.

View on ClinicalTrials.gov

Summary

The purpose of this study is to determine the safety and tolerability of monotherapy CR-002 and to identify the MTD and/or optimal biologic dose and RP2D(s) in participants with locally advanced or metastatic solid tumors.

Official title: A Phase 1/2, Multicenter, Open-label, Dose Escalation and Dose Expansion Study to Evaluate the Safety, Pharmacokinetics, and Antitumor Activity of CR-002 in Adult Participants With Locally Advanced or Metastatic Solid Tumors

Key Details

Gender

All

Age Range

18 Years - Any

Study Type

INTERVENTIONAL

Enrollment

219

Start Date

2026-10-21

Completion Date

2029-01

Last Updated

2026-11-02

Healthy Volunteers

No

Interventions

DRUG

CR-002

Intravenous Infusion

Locations (3)

Clinical Study Site

Austin, Texas, United States

Clinical Study Site

Dallas, Texas, United States

Clinical Study Site

Fairfax, Virginia, United States