Study of Safety and Efficacy of RGT-61159 in Adults With Relapsed/Refractory Adenoid Cystic Carcinoma (ACC) or Colorectal Carcinoma (CRC)
NCT06462183 · Status: RECRUITING · Phase: PHASE1 · Type: INTERVENTIONAL · Enrollment: 105
Last updated 2025-11-14
Summary
Phase 1 study to evaluate safety, tolerability and anti-tumor activity of RGT-61159 in patients with ACC or CRC
Conditions
- Adenoid Cystic Carcinoma
- Colorectal Cancer
Interventions
- DRUG
-
RGT-61159
Oral MYB inhibitor
Sponsors & Collaborators
-
Rgenta Therapeutics Inc
lead INDUSTRY
Study Design
- Allocation
- NON_RANDOMIZED
- Purpose
- TREATMENT
- Masking
- NONE
- Model
- SINGLE_GROUP
Eligibility
- Min Age
- 18 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2024-08-19
- Primary Completion
- 2025-12-31
- Completion
- 2027-06-30
- FDA Drug
- Yes
Countries
- United States
- Canada
Study Locations
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