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  • NCT02815592

Active, Not Recruiting

Trial of BMS-986012 in Combination With Platinum and Etoposide - CA001-044

Updated: 12 January, 2024   |   ClinicalTrials.gov

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CONSIDERING THIS TRIAL?
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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.
Print this page CA001-044
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Trial Details

  • Phase 1

    Phase

  • Gender(s)

  • 18+

    Age Range

  • Active, Not Recruiting

Treatment Options

Study Arms
ASSIGNED INTERVENTION
Active Comparator: Active Comparator Arm 3B
Drug: Platinum, Etoposide
Experimental: Experimental Arm 1
Drug: BMS-986012, Cisplatin, Etoposide
Experimental: Experimental Arm 2
Drug: Carboplatin, BMS-986012, Etoposide
Experimental: Experimental Arm 3A
Drug: Platinum, BMS-986012, Etoposide

Key Eligibility Criteria

For more information regarding Bristol-Myers Squibb Clinical Trial participation, please visit www.BMSStudyConnect.com Inclusion Criteria: - Male and Females 18 years of age or older - Pulmonary SCLC documented by histology or cytology - Extensive disease (Stage IV) SCLC - Eastern Cooperative Oncology Group (ECOG) performance status 0 or 1 Exclusion Criteria: - Prior systemic therapy for lung cancer - Symptomatic brain metastases - Grade 2 peripheral neuropathy - Active or chronic infection with human immunodeficiency virus (HIV), hepatitis B virus (HBV), or hepatitis C virus (HCV - Other active malignancies or prior malignancy within 2 years Other protocol defined inclusion/exclusion criteria could apply

We strongly recommend you contact BMS to report Side Effects (Adverse Events)
Side Effects (Adverse Events) and other reportable events are defined here
Report Side Effects (Adverse Events) or Product Quality Complaints: Medical Information

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