Study of Safety and Efficacy of RGT-61159 in Adults With Relapsed/Refractory Adenoid Cystic Carcinoma (ACC) or Colorectal Carcinoma (CRC)
Phase 1 study to evaluate safety, tolerability and anti-tumor activity of RGT-61159 in patients with ACC or CRC
Trial Details
- NCT ID
- NCT06462183
- Phase
- PHASE1
- Sponsor
- Rgenta Therapeutics Inc
- Status
- RECRUITING
- Cancer Type
- Colorectal Cancer
- Interventions
- Locations (sample)
- Boston, Massachusetts, United States|42.35843,-71.05977
- Ann Arbor, Michigan, United States|42.27756,-83.74088
- St Louis, Missouri, United States|38.62727,-90.19789
- New York, New York, United States|40.71427,-74.00597
- New York, New York, United States|40.71427,-74.00597
Key Eligibility Criteria
- Histologically confirmed ACC or CRC
- Radiographically measurable disease as assessed per RECIST 1.1, with at least 1 site of disease that is measurable and that has not been previously…
- Patients with locally relapsed/refractory (R/R) advanced or metastatic ACC not amenable to potentially curative surgery or radiotherapy and progres…
- Patients with CRC must have locally R/R advanced or metastatic disease not amenable to potentially curative surgery or radiotherapy; must have been…
For full eligibility, visit ClinicalTrials.gov.