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

Lung Cancer

The purpose of this study is to evaluate the safety, tolerability, drug levels, and preliminary efficacy of BMS-986507 combinations in adult participants with advanced solid tumors.

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Conditions de participation

  • Sexe:

    ALL
  • Âges admissibles:

    18 and up

Critères de participation

Inclusion Criteria

* Participants must have at least one measurable lesion per response evaluation criteria in solid tumors.
* Participants must have an Eastern Cooperative Oncology Group Performance Status of 0 or 1.
* Participants must have a life expectancy of at least 3 months at the time of the first dose.

Exclusion Criteria

* Participants must not have any mixed Small Cell Lung Cancer (SCLC) and Non-Small Cell Lung Cancer (NSCLC) histology.
* Participants must not have any untreated symptomatic central nervous system (CNS) metastases.
* Participants must not have a history of serious recurrent infections.
* Participants must not have a history of severe heart disease.
* Other protocol-defined Inclusion/Exclusion criteria apply.

Lieu de l'étude

Local Institution - 0025
Local Institution - 0025
Montreal, Quebec
Canada

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Primary Contact

Site 0025

Local Institution - 0026
Local Institution - 0026
Ottawa, Ontario
Canada

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Primary Contact

Site 0026

Local Institution - 0024
Local Institution - 0024
Edmonton, Alberta
Canada

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Primary Contact

Site 0024

Local Institution - 0022
Local Institution - 0022
Montréal, Quebec
Canada

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Primary Contact

Site 0022

Local Institution - 0023
Local Institution - 0023
Ottawa, Ontario
Canada

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Centre Hospitalier de l'Université de Montréal
Centre Hospitalier de l'Université de Montréal
Montréal, Quebec
Canada

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Primary Contact

Marie Florescu, Site 0022

5148908000
Jewish General Hospital
Jewish General Hospital
Montreal, Quebec
Canada

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Primary Contact

Jennifer Friedmann, Site 0025

514340822224915
Étude parrainée par
Bristol-Myers Squibb
Participants recherchés
Plus d'informations
ID de l'étude: NCT06618287