drugset / Trial / NCT02363855

Phase 1 Dose Escalation Study of BAY 1841788 in Japanese Metastatic Castration-resistant Prostate Cancer (mCRPC) Subjects

NCT02363855

Phase 1 Completed 9 enrolled Bayer
NaSingle-groupOpen-labelTreatment

Summary

The primary objectives of this study are to investigate the safety and tolerability of BAY 1841788 in Japanese subjects with metastatic castration-resistant prostate cancer (mCRPC) and the PK of BAY 1841788 and its major metabolite BAY 1896953.

Timeline

Start
2015-02-23
Primary completion
2015-11-19
Completion
2018-01-18

Drugs

EvaluationDrugModalityDoseRoute
Subject Darolutamide Other / unclassified 300 mg
Subject Darolutamide Other / unclassified 600 mg

Indications