drugset / Trial / NCT03404791

A Study of TAR-200 in Participants With Muscle-Invasive Urothelial Carcinoma of the Bladder Who Are Ineligible for or Refuse Cisplatin-based Chemotherapy and Who Are Unfit for Radical Cystectomy

NCT03404791

Phase 1 Completed 35 enrolled Janssen Research & Development, LLC
NaSingle-groupOpen-labelTreatment

Summary

The purpose of this study is to evaluate both the safety and tolerability of up to 4 dosing cycles of TAR-200 for 21 days per dosing cycle in the induction period.

Timeline

Start
2017-11-20
Primary completion
2019-12-23
Completion
2022-09-15

Drugs

EvaluationDrugModalityDoseRoute
Subject TAR-200 Other / unclassified Other