- A Study to Evaluate the Safety, Tolerability, Drug Levels, and Preliminary Efficacy of BMS-986507 Combinations in Adult Participants With Advanced Solid Tumors — Recruiting • Phase I / Phase II • Oncology • NCT06618287.
- Trial testing safety and early effectiveness of BMS-986507 combined with other drugs in adults with advanced cancer.
Verify eligibility, endpoints and current status on the original ClinicalTrials.gov registry before acting on this summary.
- Quick orientation before opening the registry record.
- Checking recruitment status, phase and sponsor at a glance.
- Connecting this trial to nearby guidelines, Drug Science and education.
The purpose of this study is to evaluate the safety, tolerability, drug levels, and preliminary efficacy of BMS-986507 combinations in adult participants with advanced solid tumors. Conditions: Lung Cancer, Breast Cancer Interventions: BMS-986507, Osimertinib, Pembrolizumab, Nivolumab, Pumitamig Lead Sponsor: Bristol-Myers Squibb Planned Enrollment: 416 participants