drugset / Trial / NCT04033328

Study of ORIC-101 in Combination With Enzalutamide

NCT04033328

Phase 1 Terminated 41 enrolled ORIC Pharmaceuticals
Non-randomizedSequentialOpen-labelTreatment

Summary

The purpose of this study is to establish the recommended phase 2 dose (RP2D), safety, pharmacokinetics (PK), pharmacodynamics (PD), and preliminary antitumor activity of ORIC-101 in combination with enzalutamide (Xtandi®) when administered to patients with metastatic prostate cancer progressing on enzalutamide.

Timeline

Start
2019-10-28
Primary completion
2022-11-22
Completion
2023-12-04

Drugs

EvaluationDrugModalityDoseRoute
Subject ORIC-101 Small molecule 80 mg Oral
Subject ORIC-101 Small molecule 240 mg Oral
Background Enzalutamide Other / unclassified 160 mg Oral

Indications