OncoMatch

OncoMatch/Clinical Trials/NCT06785636

Open-Label Study of Pocenbrodib Alone and in Combination With Abiraterone Acetate, Olaparib, or 177Lu-PSMA-617

Is NCT06785636 recruiting? Yes, currently enrolling (Jun 2026). This Phase 1/2 trial studies multiple treatments including Pocenbrodib and Cohort 2A (Pocenbrodib monotherapy), Cohort 2B (Pocenbrodib + abiraterone acetate), Cohort 2C (Pocenbrodib + olaparib), Cohort 2D (Pocenbrodib + 177Lu-PSMA-617 for mcrpc (metastatic castration-resistant prostate cancer).

Phase 1/2RecruitingPathos AI, Inc.NCT06785636Data as of Jun 2026

Treatment: Pocenbrodib · Cohort 2A (Pocenbrodib monotherapy), Cohort 2B (Pocenbrodib + abiraterone acetate), Cohort 2C (Pocenbrodib + olaparib), Cohort 2D (Pocenbrodib + 177Lu-PSMA-617This is a dose-finding study to assess the safety and preliminary antitumor activity of Pocenbrodib alone or with Abiraterone acetate, Olaparib or 177Lu-PSMA-617 in patients with metastatic castration-resistant prostrate cancer (mCRPC).

Check if I qualify

Extracted eligibility criteria

Treatments studied

Radioligand therapy

Cohort 2A (Pocenbrodib monotherapy), Cohort 2B (Pocenbrodib + abiraterone acetate), Cohort 2C (Pocenbrodib + olaparib), Cohort 2D (Pocenbrodib + 177Lu-PSMA-617

Other

Pocenbrodib

Cancer type

Prostate Cancer

Disease stage

Metastatic disease required

Demographics

Male only

Prior therapy

Cannot have received: chemotherapy

Intervention with any chemotherapy, investigational agent, or other anticancer drug, including enzalutamide, apalutamide, or darolutamide, 14 days prior to Screening or 5 half-lives from the last dose (whichever is shorter)

Cannot have received: investigational agent

Intervention with any chemotherapy, investigational agent, or other anticancer drug, including enzalutamide, apalutamide, or darolutamide, 14 days prior to Screening or 5 half-lives from the last dose (whichever is shorter)

Cannot have received: other anticancer drug (enzalutamide, apalutamide, darolutamide)

Intervention with any chemotherapy, investigational agent, or other anticancer drug, including enzalutamide, apalutamide, or darolutamide, 14 days prior to Screening or 5 half-lives from the last dose (whichever is shorter)

Structured fields extracted by AI. May contain errors — verify against the official protocol.

US trial sites

  • MemorialCare Orange Coast Medical Center · Fountain Valley, California
  • University of Colorado Health · Aurora, Colorado
  • Mount Sinai Medical Center · Miami, Florida
  • Karmanos Cancer Institute · Detroit, Michigan
  • Siteman Cancer Center · St Louis, Missouri

Showing up to 5 US sites.

See all sites on ClinicalTrials.gov →

Frequently asked questions

Is NCT06785636 currently recruiting?

Yes, this trial is currently recruiting patients.

Are there prior therapy exclusions?

Yes. Prior chemotherapy, investigational agent, other anticancer drug disqualifies patients from enrollment.

Is this trial open to female patients?

No. This trial enrolls male patients only.

Could you qualify for this trial?

Enter your biomarker results to see how this trial's eligibility criteria match your specific cancer profile.

Check if I qualify