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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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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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