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 CancerThe 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 - 0164Rimouski, Quebec
Canada
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Site 0164
Local Institution - 0193
Local Institution - 0193Toronto, Ontario
Canada
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Site 0193
Local Institution - 0304
Local Institution - 0304Kelowna, British Columbia
Canada
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Site 0304
Local Institution - 0093
Local Institution - 0093Chicoutimi, Quebec
Canada
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Site 0093
Local Institution - 0151
Local Institution - 0151Halifax, Nova Scotia
Canada
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Local Institution - 0150
Local Institution - 0150Québec, Quebec
Canada
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Local Institution - 0152
Local Institution - 0152Vancouver, British Columbia
Canada
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Site 0152
Local Institution - 0305
Local Institution - 0305Montréal, Quebec
Canada
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Site 0305
Sunnybrook Research Institute
Sunnybrook Research InstituteToronto, Ontario
Canada
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Daniel Khalaf, Site 0193
6048776000 ext676122Centre 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-JésusQuébec, Quebec
Canada
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Frederic Pouliot, Site 0150
4185254444BC Cancer Vancouver
BC Cancer VancouverVancouver, British Columbia
Canada
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Kim Chi, Site 0152
6048776000Jewish General Hospital
Jewish General HospitalMontreal, Quebec
Canada
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April Rose, Site 0149
41694645015190McGill University Health Centre
McGill University Health CentreMontreal, Quebec
Canada
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Ramy Saleh, Site 0305
5149341934CIUSSS- saguenay-Lac-Saint-Jean
CIUSSS- saguenay-Lac-Saint-JeanChicoutimi, Quebec
Canada
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Jose Luiz Guimaraes, Site 0093
418541-1000Centre 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 RimouskiRimouski, Quebec
Canada
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Samuel Nadeau, Site 0164
4187243000BC Cancer Kelowna
BC Cancer KelownaKelowna, British Columbia
Canada
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Daygen Finch, Site 0304
- Study Sponsored By
- Celgene
- Participants Required
- More Information
- Study ID:
NCT06764485