OncoMatch

OncoMatch/Clinical Trials/NCT06879041

A Phase I Study of [225Ac]-AZD2284 in Patients With Metastatic Castration-Resistant Prostate Cancer

Is NCT06879041 recruiting? Yes, currently enrolling (Sep 2026). This Phase 1 trial studies multiple treatments including AZD2287 and AZD2275 for metastatic castration-resistant prostate cancer.

Phase 1RecruitingAstraZenecaNCT06879041Data as of Sep 2026Location: United States · Australia · South Africa

Treatment: AZD2287 · AZD2275 · AZD2284The main purpose of the study is to assess the safety and tolerability of AZD2284, AZD2287, and AZD2275.

Check if I qualify

Extracted eligibility criteria

Treatments studied

Other

AZD2287AZD2275AZD2284

Cancer type

Prostate Cancer

Biomarker criteria

Allowed: BRCA1 mutation

A poly (adp-ribose) polymerase (PARP) inhibitor for participants with known BRCA mutation

Allowed: BRCA2 mutation

A poly (adp-ribose) polymerase (PARP) inhibitor for participants with known BRCA mutation

Disease stage

Metastatic disease required

Performance status

ECOG 0–1(Restricted strenuous activity)

Demographics

Male only

Prior therapy

Must have received: androgen receptor pathway inhibitor — mCRPC

At least 1 androgen receptor pathway inhibitor (ARPI)

Must have received: PARP inhibitor — mCRPC with BRCA mutation

A poly (adp-ribose) polymerase (PARP) inhibitor for participants with known BRCA mutation

Must have received: checkpoint inhibitor — mCRPC with MSI-H, dMMR, or TMB ≥ 10 mut/Mb

A checkpoint inhibitor for participants with known microsatellite instability-high (MSI-H), deficient mismatch pair (dMMR), or tumor mutational burden (TMB) ≥ 10 mut/Mb

Cannot have received: cytotoxic chemotherapy for CRPC

Exception: Taxanes for metastatic hormone sensitive prostate cancer (mHSPC) is acceptable if the last cycle Day 1 was > 12 months before first study treatment

No previous cytotoxic chemotherapy for CRPC. Taxanes for metastatic hormone sensitive prostate cancer (mHSPC) is acceptable if the last cycle Day 1 was > 12 months before first study treatment.

Lab requirements

Blood counts

Kidney function

Liver function

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

US trial sites

  • Research Site · Palo Alto, California
  • Research Site · San Diego, California
  • Research Site · Miami, Florida
  • Research Site · Tampa, Florida
  • Research Site · Chicago, Illinois

Showing up to 5 US sites.

See all sites on ClinicalTrials.gov →

Frequently asked questions

Is NCT06879041 currently recruiting?

Yes, this trial is currently recruiting patients.

Are there prior therapy exclusions?

Yes. Prior cytotoxic chemotherapy for CRPC 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