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NCT06067841RecruitingPhase 1

A Study to Assess BMS-986460 in Participants With Metastatic Castration-resistant Prostate Cancer

A Phase 1, Open-label Study of BMS-986460 in Participants With Metastatic Castration-resistant Prostate Cancer

Source: ClinicalTrials.gov · Last updated 10 Aug 2026

Brief summary (registry, in English)

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.

Status (registry)
Recruiting
Phase (registry)
Phase 1
Study type
Interventional
Enrollment
140 (estimated)
First submitted
28 Sept 2023
Start date
18 Oct 2023
Primary completion date
24 Aug 2029
Lead sponsor
Bristol-Myers Squibb
NCT number
NCT06067841
EU CT number
2024-513987-24-00
EudraCT number
2024-513987-24

What you commit to

  • Study type: Interventional · Phase 1
  • Planned participants: 140
  • From 18 Oct 2023 to the primary completion date, 24 Aug 2029
  • 15 sites in 3 countries
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other illness

  • Participant must not have history of brain metastases.
  • Participant must not have impaired cardiac function or clinically significant cardiac disease.

Lab values

  • Participant must not have any significant medical condition, including active or uncontrolled infection, psychiatric illness, or the presence of laboratory abnormalities, which places the participant at unacceptable risk or prevent participation in the study based on Investigator assessment.
    • Other protocol-defined inclusion/exclusion criteria apply

Who the study is looking for

  • 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-resistant prostate cancer (CRPC)

Age in the registry: 18 years to - · Sex: Male · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (15)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
-
Coordinator of this site? Confirm its status
MontrealCanadaNot yet recruiting
-
Coordinator of this site? Confirm its status
TorontoCanadaNot yet recruiting
Institut Bergonie
Coordinator of this site? Confirm its status
BordeauxFranceRecruiting
Centre Leon Berard
Coordinator of this site? Confirm its status
LyonFranceRecruiting
Institut Paoli-Calmettes
Coordinator of this site? Confirm its status
MarseilleFranceRecruiting
Assistance Publique Hopitaux de Paris
Coordinator of this site? Confirm its status
ParisFranceRecruiting
Institut Gustave Roussy
Coordinator of this site? Confirm its status
VillejuifFranceRecruiting
Dana-Farber Cancer Institute
Coordinator of this site? Confirm its status
BostonUnited StatesRecruiting
Duke Cancer Institute
Coordinator of this site? Confirm its status
DurhamUnited StatesRecruiting
Memorial Sloan-Kettering Cancer Center
Coordinator of this site? Confirm its status
New YorkUnited StatesRecruiting
Stanford Cancer Center
Coordinator of this site? Confirm its status
Palo AltoUnited StatesRecruiting
-
Coordinator of this site? Confirm its status
San AntonioUnited StatesWithdrawn
NEXT Oncology
Coordinator of this site? Confirm its status
San AntonioUnited StatesRecruiting
Florida Cancer Specialists Sarasota Drug Development Unit
Coordinator of this site? Confirm its status
SarasotaUnited StatesRecruiting
Fred Hutchinson Cancer Center
Coordinator of this site? Confirm its status
SeattleUnited StatesRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.