OncoMatch/Clinical Trials/NCT07332455
First-Time-in-Human Study of GSK5471713 in Adults With mCRPC
Is NCT07332455 recruiting? Yes, currently enrolling (Jun 2026). This Phase 1/2 trial studies GSK5471713 for neoplasms, prostate.
Treatment: GSK5471713 — This first-time-in-human study will evaluate the safety, tolerability, pharmacokinetics, pharmacodynamics, preliminary clinical activity, and establish the benefit/risk of GSK5471713 given as a monotherapy in mCRPC.
Check if I qualifyExtracted eligibility criteria
Treatments studied
Other
Disease stage
Metastatic disease required
Performance status
ECOG 0–1(Restricted strenuous activity)
Demographics
Prior therapy
Must have received: androgen deprivation therapy
prostate cancer progression while on Androgen deprivation therapy (ADT)
Must have received: androgen receptor pathway inhibitor — Hormone-Sensitive Prostate Cancer (HSPC) or Castration resistant prostate cancer (CRPC)
progression on ADT and >=1 prior Androgen receptor pathway inhibitors (ARPI) for Hormone-Sensitive Prostate Cancer (HSPC) or Castration resistant prostate cancer (CRPC)
Must have received: taxane
received 1-2 prior taxane based chemotherapy regimens
Cannot have received: androgen receptor degrader
Prior therapy with Androgen receptor (AR) Degrader targeted therapy
Lab requirements
Cardiac function
Impaired cardiac function or clinically significant cardiac disease [excluded]
Impaired cardiac function or clinically significant cardiac disease
Structured fields extracted by AI. May contain errors — verify against the official protocol.
US trial sites
- GSK Investigational Site · Grand Rapids, Michigan
- GSK Investigational Site · West Valley City, Utah
Showing up to 5 US sites.
See all sites on ClinicalTrials.gov →Frequently asked questions
Is NCT07332455 currently recruiting?
Yes, this trial is currently recruiting patients.
Are there prior therapy exclusions?
Yes. Prior androgen receptor degrader 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