Clinical Trial

Minimal Residual Disease Used in Predicting Therapeutic Efficacy in Metastatic Hormone-sensitive Prostate Cancer

Not Yet Recruiting
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Summary
This study is a prospective, single-center, observational study of patients with newly diagnosed metastatic hormone-sensitive prostate cancer (mHSPC). Minimal residual disease (MRD) detection is used to investigate the actual efficacy responses of mHSPC patients with different gene mutation characteristics to treatment regimens. Factors influencing efficacy are further analyzed to provide a basis for the precise clinical diagnosis and treatment of mHSPC patients.
Protocol Amendment History 2 amendments
This ClinicalTrials.gov record has been amended 2 times since 2025-08-02; most recent amendment 2026-01-08.
Trial Details
NCT Number NCT07112612
Lead Sponsor Anhui Medical University
Conditions MRD, Prostate Cancer, mHSPC
Enrollment 50 participants
Start Date 2026-01-30
Primary Completion 2026-12-30 (estimated)
Study Completion 2027-04-30 (estimated)
Updated on ClinicalTrials.gov 2026-01-12