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Rechercher Study Connect
  • NCT06094296

Recruiting

A Study of BMS-986315 and Nivolumab in Combination With Chemotherapy in Participants With First-line Stage IV or Recurrent Non-small Cell Lung Cancer (NSCLC) - CA047-1009

Mis à jour: 5 mars, 2024   |   ClinicalTrials.gov

Résumé imprimable

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SÉLECTIONNER LA LANGUE

Détails de l’essai

  • Phase 2

    Phase

  • Sexe(s)

  • 18+

    Tranche d’âge

  • 15

    Site(s)

  • Recruiting

Options de traitement

Bras de l’étude
INTERVENTION ASSIGNÉE
Experimental: Part 1: BMS-986315 DL 2 + Nivolumab + Histology-based PDCT
Drug: Paclitaxel, Cisplatin, Pemetrexed, BMS-986315, Carboplatin
Experimental: Part 1: BMS-986315 Dose Level (DL) 1 + Nivolumab + Histology-based PDCT
Drug: BMS-986315, Pemetrexed, Paclitaxel, Carboplatin, Cisplatin
Experimental: Part 2: BMS-986315 DL 1 + Nivolumab + Histology-based PDCT
Drug: BMS-986315, Nivolumab, Paclitaxel, Cisplatin, Carboplatin, Pemetrexed
Experimental: Part 2: BMS-986315 DL 2 + Nivolumab + Histology-based PDCT
Drug: BMS-986315, Nivolumab, Paclitaxel, Cisplatin, Carboplatin, Pemetrexed
Active Comparator: Part 2: Nivolumab + Histology-based PDCT
Drug: Nivolumab, Pemetrexed, Paclitaxel, Carboplatin, Cisplatin

Principaux critères d’éligibilité

Inclusion Criteria: - Participants must have NSCLC with Stage IV or recurrent disease following multimodal therapy for locally advanced disease. - Study treatment must be first-line therapy for Stage IV or recurrent disease. - Participants in all parts of the study must have: - measurable disease per Response Evaluation Criteria in Solid Tumors version 1.1. (RECIST v1.1) - an Eastern Cooperative Oncology Group (ECOG) Performance Status of 0 or 1 - a life expectancy of at least 3 months at the time of first dose Exclusion Criteria: - Untreated symptomatic central nervous system metastases - Participants with epidermal growth factor receptor (EGFR)/ALK receptor tyrosine kinase (ALK)/ROS proto-oncogene 1 (ROS1)/neurotrophic tyrosine receptor kinase (NTRK)/MET proto-oncogene (MET)/B-Raf proto-oncogene (BRAF)/RET proto-oncogene (RET) mutations amenable to targeted therapies - Participants with any known medical condition that, in the investigator's opinion, would increase the risk associated with study participation or study drug administration or interfere with the interpretation of safety results Note: Other protocol-defined inclusion/exclusion criteria apply.

Nous vous recommandons vivement de contacter BMS pour signaler les effets secondaires (événements indésirables)
Les effets secondaires (événements indésirables) et les autres événements à signaler sont définis ici
Signaler des plaintes concernant des effets indésirables (effets indésirables) ou des produits: Informations médicales