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Clinical Trial ● Currently Recruiting Phase I / Phase II NCT06618287

A Study to Evaluate the Safety, Tolerability, Drug Levels, and Preliminary Efficacy of BMS-986507 Combinations in Adult Participants With Advanced Solid Tumors

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 /…

📅 07 May 2026 ⏱ 1 min read
Currently Recruiting
This trial is actively seeking participants in the UK. Discuss eligibility with your patient before referring.
Status
Currently Recruiting
Phase
Phase I / Phase II
NCT ID
NCT06618287
Start
2025-02-04
Completion
2031-02-26
ClinicaliQ Trial Snapshot
  • 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.

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  • Connecting this trial to nearby guidelines, Drug Science and education.
What This Trial Is Studying

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

Full Trial Details
View this trial on the source registry
Eligibility criteria, protocol, and results when available
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