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RECRUITING
NCT07335497
PHASE1/PHASE2

CR-001 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-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.

Official title: A Phase 1/2, Multicenter, Open-label, Dose Escalation and Dose Expansion Study to Evaluate the Safety, Pharmacokinetics, Pharmacodynamics, and Antitumor Activity of CR-001 in Adult Participants With Locally Advanced or Metastatic Solid Tumors

Key Details

Gender

All

Age Range

18 Years - Any

Study Type

INTERVENTIONAL

Enrollment

290

Start Date

2026-02-17

Completion Date

2029-02

Last Updated

2026-02-19

Healthy Volunteers

No

Interventions

DRUG

CR-001

Intravenous Infusion

Locations (5)

Clinical Study Site

Denver, Colorado, United States

Clinical Study Site

Orlando, Florida, United States

Clinical Study Site

Sarasota, Florida, United States

Clinical Study Site

Nashville, Tennessee, United States

Clinical Study Site

Dallas, Texas, United States