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NCT06067841
A Study to Assess BMS-986460 in Participants With Metastatic Castration-resistant Prostate Cancer
The purpose of this study is to assess the safety, tolerability, and preliminary efficacy of BMS-986460 in men with Metastatic Castration-resistant Prostate Cancer.
Trial Details
NCT ID NCT06067841
Phase PHASE1
Sponsor Bristol-Myers Squibb
Status RECRUITING
Cancer Type Prostate Cancer
Interventions
Locations (sample) Palo Alto, California, United States|37.44188,-122.14302 Sarasota, Florida, United States|27.33643,-82.53065 Boston, Massachusetts, United States|42.35843,-71.05977 New York, New York, United States|40.71427,-74.00597 Durham, North Carolina, United States|35.99403,-78.89862
Key Eligibility Criteria
Participant must have histologically or cytologically confirmed adenocarcinoma of the prostate. Participant must have an Eastern Cooperative Oncology Group (ECOG) performance status 0 to 1. Participant must have prostate specific antigen (PSA) of ≥ 2 ng/mL at Screening Participant must have progressed on androgen deprivation therapy (ADT) and at least one prior secondary hormonal therapy approved for castration-re…
For full eligibility, visit ClinicalTrials.gov .
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