A Study of HRS-5041 Tablets Combined With Antitumor Therapy in Subjects With Advanced Prostate Cancer

The purpose of this study is to evaluate the efficacy, and safety of HRS-5041 tablets combined with antitumor therapy in subjects with advanced prostate cancer.

Trial Details

NCT ID
NCT06568094
Phase
PHASE1 / PHASE2
Sponsor
Jiangsu HengRui Medicine Co., Ltd.
Status
RECRUITING
Cancer Type
Prostate Cancer
Interventions
  • HRS-5041 tablets
  • Abiraterone Acetate tablets(II)
  • Prednisone Acetate tablets
  • Docetaxel Injection
  • HRS-1167 tablets
  • SHR2554 tablets
Locations (sample)
  • Harbin, Heilongjiang, China|45.75,126.65
  • Shanghai, Shanghai Municipality, China|31.22222,121.45806

Key Eligibility Criteria

  • Have the ability to give informed consent, and are willing and able to comply with planned visits for medical examinations and other procedural req…
  • The age is above 18 years old when signing the informed consent (the ceiling age is 80 years old in the dose escalation phase), male.
  • ECOG score is 0 or 1.
  • An expected survival of ≥ 12 weeks.

For full eligibility, visit ClinicalTrials.gov.

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