drugset / Trial / NCT07407283

A Clinical Study of SHR-4394 in Combination With Anti-tumor Therapy in Prostate Cancer

NCT07407283

Phase 1/2 Recruiting 100 enrolled Jiangsu HengRui Medicine Co., Ltd.
NaSingle-groupOpen-labelTreatment

Summary

The study aims to assess the safety and tolerability of SHR-4394 in combination with anti-tumor therapy in participants with prostate cancer, and determine the recommended Phase II dose (RP2D); To evaluate of the efficacy of SHR-4394 in combination with anti-tumor therapy in participants with prostate cancer based on Prostate-Specific Antigen (PSA) response rate.

Timeline

Start
2026-04-08
Primary completion
2027-11
Completion
2028-04

Drugs

EvaluationDrugModalityDoseRoute
Subject SHR4394 Unknown
Background HRS-5041 Other / unclassified
Background Rezvilutamide Small molecule
Background Tazemetostat Small molecule

Indications