drugset / Trial / NCT01613118

Randomized, Double-Blind, Safety and Efficacy Study of RE-021 (Sparsentan) in Focal Segmental Glomerulosclerosis

NCT01613118

Phase 2 Completed 109 enrolled Travere Therapeutics, Inc.
RandomizedParallel-groupDouble-blindTreatment

Summary

This study will investigate whether RE-021 (Sparsentan), a selective dual-acting receptor antagonist with affinity for endothelin (A type) and angiotensin II receptors (Type 1), is safe and effective in treating patients with focal segmental glomerulosclerosis (FSGS).

Timeline

Start
2014-03
Primary completion
2016-06
Completion
2024-03-25

Publications

Drugs

EvaluationDrugModalityDoseRoute
Comparator Irbesartan Small molecule 150 mg Oral
Comparator Irbesartan Small molecule 300 mg Oral
Subject Sparsentan Small molecule 200 mg Oral
Subject Sparsentan Small molecule 400 mg Oral
Subject Sparsentan Small molecule 800 mg Oral