drugset / Trial / NCT07516704

Safety and Efficacy of Docetaxel, Darolutamide, and Homoharringtonine Combined With Androgen Deprivation Therapy in Neoadjuvant Treatment of High-Risk Prostate Cancer: A Multicenter Prospective, Single-Arm Clinical Study

NCT07516704

Phase 0 Not yet recruiting 94 enrolled Zhongda Hospital
NaSingle-groupOpen-labelTreatment

Summary

Previous study findings suggest that the efficacy limitations of the neoadjuvant treatment regimen combining docetaxel with androgen deprivation therapy are associated with protein synthesis. Homoharringtonine (HHT) is currently the only small-molecule translation elongation inhibitor approved by the U.S. Food and Drug Administration (FDA). Building on this foundation, we plan to conduct a prospective interventional study aimed at validating whether the intensified quadruple regimen, formed by adding darolutamide and homoharringtonine (HHT) to the standard regimen, can further significantly enhance the depth of pathological response and improve patient outcomes through multi-mechanism synergy.

Timeline

Start
2026-04-01
Primary completion
2027-12-01
Completion
2027-12-12

Drugs

EvaluationDrugModalityDoseRoute
Subject Darolutamide Other / unclassified 600 mg Oral
Subject Docetaxel Small molecule 75 mg/m2 Intravenous
Subject Goserelin Other / unclassified 3.6 mg Subcutaneous
Subject Homoharringtonine Small molecule 1 mg Intravenous

Indications