drugset / Trial / NCT04498702

Study of Continuous APL-1202 Treatment in Subjects With High-Risk Non-Muscle-Invasive Bladder Cancer (NMIBC) Relapsed From Intravesical Chemo/BCG Therapy

NCT04498702

Phase 2 Completed 41 enrolled Jiangsu Yahong Meditech Co., Ltd aka Asieris
NaSingle-groupOpen-labelTreatment

Summary

To determine the efficacy of oral APL-1202 administered consecutively for 12 weeks in subjects with high-risk NMIBC relapsed from intravesical chemo/BCG therapy based on the recurrence-free rate (RFR) at 12 months after APL-1202 treatment.

Timeline

Start
2014-05-13
Primary completion
2017-01-18
Completion
2017-01-18

Drugs

EvaluationDrugModalityDoseRoute
Subject APL-1202 Unknown 300 mg Oral
Subject APL-1202 Unknown 450 mg Oral
Subject APL-1202 Unknown 600 mg Oral
Subject APL-1202 Unknown 750 mg Oral