drugset / Trial / NCT03497429

A Study of Niraparib as Single Agent in Participants With Advanced Solid Tumors

NCT03497429

Phase 1 Completed 9 enrolled Takeda
Non-randomizedSequentialOpen-labelOther

Summary

The purpose of this study is to evaluate the safety, tolerability and pharmacokinetics of Niraparib in Japanese participants with advanced solid tumors.

Timeline

Start
2018-04-05
Primary completion
2020-02-10
Completion
2020-02-10

Drugs

EvaluationDrugModalityDoseRoute
Subject Niraparib Small molecule 200 mg Oral
Subject Niraparib Small molecule 300 mg Oral

Indications