A Study to Evaluate the Safety, Tolerability, Drug Levels, and Preliminary Efficacy of BMS-986507 Combinations in Adult Participants With Advanced Solid Tumors
Lung CancerThe 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
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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 - 0025Montreal, Quebec
Canada
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Site 0025
Local Institution - 0026
Local Institution - 0026Ottawa, Ontario
Canada
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Site 0026
Local Institution - 0024
Local Institution - 0024Edmonton, Alberta
Canada
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Site 0024
Local Institution - 0022
Local Institution - 0022Montréal, Quebec
Canada
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Site 0022
Local Institution - 0023
Local Institution - 0023Ottawa, Ontario
Canada
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Centre Hospitalier de l'Université de Montréal
Centre Hospitalier de l'Université de MontréalMontréal, Quebec
Canada
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Marie Florescu, Site 0022
5148908000Jewish General Hospital
Jewish General HospitalMontreal, Quebec
Canada
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Jennifer Friedmann, Site 0025
514340822224915- Étude parrainée par
- Bristol-Myers Squibb
- Participants recherchés
- Plus d'informations
- ID de l'étude:
NCT06618287