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A Study to Compare the Combination of Navlimetostat (BMS-986504) With Pembrolizumab and Chemotherapy Versus Placebo Plus Pembrolizumab and Chemotherapy in First-line Metastatic Non-small Cell Lung Cancer Participants With Homozygous MTAP Deletion
RECRUITINGPhase 2/3Sponsored by Bristol-Myers Squibb
Actively Recruiting
PhasePhase 2/3
SponsorBristol-Myers Squibb
Started2026-01-02
Est. completion2031-08-12
Eligibility
Age18 Years+
Healthy vol.Accepted
Locations42 sites
View on ClinicalTrials.gov →
NCT07063745
Summary
The purpose of this study is to compare the clinical benefit of the combination of Navlimetostat (BMS-986504) (a selective MTA-cooperative inhibitor of PRMT5) plus pembrolizumab and chemotherapy versus placebo plus pembrolizumab and chemotherapy in first-line metastatic non-small cell lung cancer participants with homozygous MTAP deletion
Eligibility
Age: 18 Years+Healthy volunteers accepted
Inclusion Criteria * Participants must have Metastatic (Stage IV or recurrent) non-small cell lung cancer (NSCLC) (as defined by the American Joint Committee on Cancer, Ninth Edition) with no prior systemic anti-cancer therapy for metastatic disease. * Participants must have histologically confirmed diagnosis of NSCLC and homozygous methylthioadenosine phosphorylase (MTAP) deletion or MTAP loss. * Participants must have an Eastern Cooperative Oncology Group (ECOG) performance status of 0-1. * Participants must have at least 1 measurable lesion as per RECIST v1.1. Exclusion Criteria * Nonsquamous participants must not have documented targetable oncogenic mutation or actionable genetic alterations (AGAs) for which there is a standard of care (SoC) available as first-line (1L) therapy. * Participants must not have symptomatic brain metastases or spinal cord compression. * Participants must not have any prior systemic therapy (chemotherapy, immunotherapy, targeted therapy, or biological therapy) for metastatic non-small cell lung cancer (mNSCLC). Note: One cycle of SoC treatment prior to randomization will be allowed for participants who require immediate treatment if clinically indicated. * Participants must not have any known or suspected impairment of gastrointestinal function that may prohibit the ability to absorb or swallow an oral medication without chewing or crushing. * Other protocol-defined Inclusion/Exclusion criteria apply.
Conditions3
CancerLung CancerMetastatic Non-small Cell Lung Cancer With MTAP Deletion
Interventions7
Locations42 sites
Alaska Oncology and Hematology
Anchorage, Alaska, 99508
Steven Liu, Site 0119907-257-9851
Highlands Oncology Group
Springdale, Arkansas, 72762
Eric Schaefer, Site 0135479-872-8130
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Trial data from ClinicalTrials.gov. Trial status and eligibility can change — verify directly with the study contact or on ClinicalTrials.gov.
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Actively Recruiting
PhasePhase 2/3
SponsorBristol-Myers Squibb
Started2026-01-02
Est. completion2031-08-12
Eligibility
Age18 Years+
Healthy vol.Accepted
Locations42 sites
View on ClinicalTrials.gov →
NCT07063745