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CR-002 in Adult Participants With Locally Advanced or Metastatic Solid Tumors
Sponsor: Crescent Biopharma, Inc.
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
Conditions
Interventions
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