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Active, Not Recruiting

A Study of BMS-986207 Given Alone and in Combination With Nivolumab or With Nivolumab and Ipilimumab in Advanced Solid Tumors - CA020-002

Updated: 14 September, 2023   |   ClinicalTrials.gov

Print Friendly Summary

CONSIDERING THIS TRIAL?
Print this page and the trial guide to help you talk with your doctor.
Use the Study Participant's Guide to navigate the process of participating in a clinical trial. Understand key factors to consider before deciding and get questions to ask your healthcare team.

Trial Details

  • Phase 1/Phase 2

    Phase

  • Gender(s)

  • 18+

    Age Range

  • Active, Not Recruiting

Treatment Options

Study Arms
ASSIGNED INTERVENTION
Experimental: Part 1A: Dose Escalation Monotherapy
Drug: BMS-986207
Experimental: Part 1B: Dose Escalation Combination Therapy
Biological: Nivolumab Drug: BMS-986207
Experimental: Part 1C: Triplet Cohort
Drug: BMS-986207 Biological: Ipilimumab Biological: Nivolumab
Experimental: Part 2A: Expansion Monotherapy
Drug: BMS-986207
Experimental: Part 2B: Expansion Combination Therapy
Biological: Nivolumab Drug: BMS-986207
Experimental: Part 2C: Triplet Expansion
Drug: BMS-986207 Biological: Ipilimumab Biological: Nivolumab

Key Eligibility Criteria

Inclusion Criteria: - Must have pre-existing or prior programmed death-ligand 1 (PD-L1) immunohistochemistry (IHC) results within 3 months of enrollment from testing of tumor tissue; PD-L1 expression must be tumor cell positive ≥ 1% for a participant to be eligible for enrollment - Eastern Cooperative Oncology Group (ECOG) performance status of 0 or 1 - Measurable disease by computed tomography (CT) or magnetic resonance imaging (MRI) per Response Evaluation Criteria in Solid Tumors (RECIST) v1.1 criteria; radiographic tumor assessment performed within 28 days before randomization Exclusion Criteria: - Primary central nervous system (CNS) disease, or tumors with CNS metastases as the only site of disease. Controlled brain metastases will be allowed to enroll - Other active malignancy requiring concurrent intervention - Uncontrolled or significant cardiovascular disease - Active, known, or suspected autoimmune disease - NSCLC without prior treatment in the advanced or metastatic setting (Part 2C) Other protocol-defined inclusion/exclusion criteria apply

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