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A Study to Compare the Efficacy and Safety of BMS-986365 Versus the Investigator's Choice of Therapy in Participants With Metastatic Castration-resistant Prostate Cancer

Metastatic Castration-resistant Prostate Cancer

The purpose of this study is to compare the efficacy and safety of BMS-986365 versus the investigator's choice of therapy in participants with Metastatic Castration-resistant Prostate Cancer.

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Participation Requirements

  • Sex:

    MALE
  • Eligible Ages:

    18 and up

Participation Criteria

Inclusion Criteria

* Participants must have histologic or cytologic confirmation of adenocarcinoma of the prostate without small cell or neuro-endocrine features.
* Participants must have current evidence of metastatic disease documented by either bone lesions on radionuclide bone scan and/or soft tissue lesions on computed tomography/magnetic resonance imaging (CT/MRI).
* Participants must be asymptomatic or mildly symptomatic from prostate cancer with score on Brief Pain Inventory - Short Form (BPI-SF) that must be \< 4.
* Participants must have had previous treatment with an androgen receptor pathway inhibitor (abiraterone, enzalutamide, apalutamide, or darolutamide).

Exclusion Criteria

* Participants must not have impaired cardiac function or clinically significant cardiac disease.
* Participants must not have any brain metastasis.
* Participants must not have any liver metastasis.
* Participants with superscan on technetium-99m (Tc-99m) radionuclide bone scans.
* Other protocol-defined Inclusion/Exclusion criteria apply.

Study Location

Local Institution - 0164
Local Institution - 0164
Rimouski, Quebec
Canada

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Primary Contact

Site 0164

Local Institution - 0193
Local Institution - 0193
Toronto, Ontario
Canada

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Primary Contact

Site 0193

Local Institution - 0304
Local Institution - 0304
Kelowna, British Columbia
Canada

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Primary Contact

Site 0304

Local Institution - 0093
Local Institution - 0093
Chicoutimi, Quebec
Canada

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Primary Contact

Site 0093

Local Institution - 0151
Local Institution - 0151
Halifax, Nova Scotia
Canada

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Local Institution - 0150
Local Institution - 0150
Québec, Quebec
Canada

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Local Institution - 0152
Local Institution - 0152
Vancouver, British Columbia
Canada

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Primary Contact

Site 0152

Local Institution - 0305
Local Institution - 0305
Montréal, Quebec
Canada

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Primary Contact

Site 0305

Sunnybrook Research Institute
Sunnybrook Research Institute
Toronto, Ontario
Canada

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Primary Contact

Daniel Khalaf, Site 0193

6048776000 ext676122
Centre intégré de cancérologie du CHU de Québec Université Laval, Hôpital de l'Enfant-Jésus
Centre intégré de cancérologie du CHU de Québec Université Laval, Hôpital de l'Enfant-Jésus
Québec, Quebec
Canada

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Primary Contact

Frederic Pouliot, Site 0150

4185254444
BC Cancer Vancouver
BC Cancer Vancouver
Vancouver, British Columbia
Canada

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Primary Contact

Kim Chi, Site 0152

6048776000
Jewish General Hospital
Jewish General Hospital
Montreal, Quebec
Canada

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Primary Contact

April Rose, Site 0149

41694645015190
McGill University Health Centre
McGill University Health Centre
Montreal, Quebec
Canada

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Primary Contact

Ramy Saleh, Site 0305

5149341934
CIUSSS- saguenay-Lac-Saint-Jean
CIUSSS- saguenay-Lac-Saint-Jean
Chicoutimi, Quebec
Canada

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Primary Contact

Jose Luiz Guimaraes, Site 0093

418541-1000
Centre intégré de santé et de services sociaux du Bas Saint-Laurent- Hôpital régional de Rimouski
Centre intégré de santé et de services sociaux du Bas Saint-Laurent- Hôpital régional de Rimouski
Rimouski, Quebec
Canada

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Primary Contact

Samuel Nadeau, Site 0164

4187243000
BC Cancer Kelowna
BC Cancer Kelowna
Kelowna, British Columbia
Canada

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Primary Contact

Daygen Finch, Site 0304

Study Sponsored By
Celgene
Participants Required
More Information
Study ID: NCT06764485