drugset / Trial / NCT02841995

A Study to Evaluate the Safety, Tolerability, and Activity of KD025 in Subjects With Chronic Graft Versus Host Disease

NCT02841995

Phase 2 Completed 54 enrolled Kadmon, a Sanofi Company
Non-randomizedParallel-groupOpen-labelTreatment

Summary

This study was been conducted to evaluate the safety, tolerability, and activity of belumosudil (formerly known as KD025) in adult participants with chronic graft versus host disease (cGVHD).

Timeline

Start
2016-09-15
Primary completion
2022-05-12
Completion
2022-05-12

Drugs

EvaluationDrugModalityDoseRoute
Subject Belumosudil Small molecule 200 mg Oral
Subject Belumosudil Small molecule 400 mg Oral