Phase 1 Prostate Cancer Trial, Recruiting NCT06067841 Sponsor: Bristol-Myers Squibb Condition: Prostate Cancer
Back to Prostate Cancer

Phase 1 Prostate Cancer Trial, Recruiting

NCT06067841
Recruiting Phase 1

Who may be able to join

AI generated eligibility summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI

Who might be able to join this trial:

  • People who have been diagnosed with prostate cancer (specifically the type called adenocarcinoma), confirmed through a tissue or cell sample.
  • People who are generally able to carry out daily activities with no or minimal limitations (based on a standard medical scale called ECOG, scored 0 or 1).
  • People whose PSA (a protein measured in the blood that can indicate prostate cancer activity) is at least 2 ng/mL at the time of screening.
  • People whose prostate cancer has continued to grow or spread despite hormone-lowering therapy (ADT) and at least one other approved hormonal treatment for castration-resistant prostate cancer.

Who may not be able to join:

  • People who have a history of cancer that has spread to the brain.
  • People who have reduced heart function or a significant heart condition.
  • People who have a serious medical condition — such as an active or uncontrolled infection, a mental health condition, or abnormal laboratory results — that the supervising doctor believes would make participation unsafe or not possible.

Important: Other eligibility criteria set out in the trial protocol may also apply, and the trial site is the appropriate contact for confirming whether a person meets all requirements. Always verify eligibility with the trial site directly before applying.

Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.

This is a simplified plain English summary of the eligibility criteria. Full criteria are set by the trial investigators and may include additional requirements not shown here. Never self-exclude from a trial based on this summary. Contact the trial site directly to confirm your eligibility.
Last synced 28 July 2026
Phase 1: approximately ~10% of drugs entering this phase reach regulatory approval, based on published industry-wide historical data. This is not specific to this trial.
Phase success rates shown are historical industry-wide averages based on published data. They are not a prediction for this specific trial or your individual situation.

Contact this trial

Principal Investigator: Bristol-Myers Squibb, Bristol-Myers Squibb

Phone: 855-907-3286

Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.

GP referral letter

Print a one-page summary to share with your doctor.

Trial details

Status
Recruiting
Phase
Phase 1
Registry
ClinicalTrials.gov
Start date
18 October 2023
Est. completion
24 August 2029

Where this trial is recruiting

🇺🇸 United States

Primary endpoints

Number of participants with adverse events (AEs); Number of participants with serious adverse events (SAEs); Number of participants with AEs meeting protocol defined dose limiting toxicity (DLT) criteria; Number of participants with AEs leading to study intervention discontinuation; Number of deaths

Can't join this trial?

Expanded access pathways

If this trial is not available to you, other access pathways may exist. In Australia, the TGA Special Access Scheme allows access to unapproved therapeutic goods for individual patients.

TGA Special Access Scheme information

Find other recruiting trials on ClinicalTrials.gov

Data last synced from ClinicalTrials.gov: 28 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.

Trial recruitment status can change without notice between our nightly data updates. Always contact the trial site directly to confirm current recruitment status before making any decisions or travel arrangements.

View original record on ClinicalTrials.gov