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

Trial Details

NCT ID

NCT06618287

Phase

PHASE1 / PHASE2

Sponsor

Bristol-Myers Squibb

Status

RECRUITING

Cancer Type

Breast Cancer

Interventions

• BMS-986507
• Osimertinib
• Pembrolizumab
• Nivolumab
• Pumitamig

Locations (sample)

• Birmingham, Alabama, United States|33.52066,-86.80249
• Miami, Florida, United States|25.77427,-80.19366
• Iowa City, Iowa, United States|41.66113,-91.53017
• St Louis, Missouri, United States|38.62727,-90.19789
• Hackensack, New Jersey, United States|40.88593,-74.04347

Key Eligibility Criteria

• Participants must have at least one measurable lesion per response evaluation criteria in solid tumors.
• Participants must have an Eastern Cooperative Oncology Group (ECOG) Performance Status of 0 or 1.
• Participants must have a life expectancy of at least 3 months at the time of the first dose.
• Group A: Participants must have pathologically confirmed locally advanced or metastatic NSCLC with an EGFR exon 19 deletion or L858R mutation in ex…

For full eligibility, visit ClinicalTrials.gov.

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