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NCT07293351
A Study to Evaluate the Safety, Tolerability, and Efficacy of Pumitamig Alone or in Combination With Ipilimumab or Cabozantinib in Participants With Advanced Renal Cell Carcinoma (RCC) (ROSETTA RCC-208)
The purpose of this study is to evaluate the safety, tolerability, and efficacy of Pumitamig alone or in combination with Ipilimumab or Cabozantinib in participants with advanced Renal Cell Carcinoma (RCC)
Trial Details
NCT ID NCT07293351
Phase PHASE1 / PHASE2
Sponsor Bristol-Myers Squibb
Status RECRUITING
Cancer Type Kidney Cancer
Interventions Pumitamig Ipilimumab Cabozantinib
Locations (sample) Palo Alto, California, United States|37.44188,-122.14302 New Haven, Connecticut, United States|41.30815,-72.92816 Washington D.C., District of Columbia, United States|38.89511,-77.03637 Miami, Florida, United States|25.77427,-80.19366 Atlanta, Georgia, United States|33.749,-84.38798
Key Eligibility Criteria
Participants must have a histologically confirmed diagnosis of locally advanced, unresectable (not amenable to curative surgery or radiation therap… Participants must have clear cell RCC (ccRCC) or non-clear cell RCC (nccRCC) may be enrolled in Part 1. Note: Part 2 may only enroll participants w… Participants may have favorable, intermediate or poor risk disease categories. Participants must not have received prior systemic therapy for metastatic RCC, with the following exceptions:
For full eligibility, visit ClinicalTrials.gov .
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