drugset / Trial / NCT06155084

A Study to Assess the Safety, Pharmacokinetics, and Anti-Tumor Activity of Oral HP518 in mCRPC Patients

NCT06155084 ↗

Phase 1/2 Recruiting 84 enrolled Hinova Pharmaceuticals Inc.
Non-randomizedSequentialOpen-labelTreatment

Summary

The overall objective of this Phase 1 study is to evaluate the safety, PK,and anti-tumor activity of daily oral dosing with HP518,selecting the RP2D of HP518 based on assessments of patients with progressive mCRPC in dose-escalation phase

Timeline

Start
2023-12-26
Primary completion
2026-03
Completion
2026-09

Drugs

EvaluationDrugModalityDoseRoute
Subject HP518 Unknown 400 mg Oral
Subject HP518 Unknown 500 mg Oral

Indications