Project Title: |
Randomized, Double-Blind, Safety and Efficacy Study of RE-021 (Sparsentan) in Focal Segmental Glomerulosclerosis (DUET) |
Project Type: |
Clinical Trial, Enrolment terminated |
Disease group(s): |
Hereditary glomerulopathies |
Project Summary: |
The purpose of this trial is to quantify the anti-proteinuric efficacy and to profile the safety of Sparsentan administration in patients with FSGS. |
Lead principal investigator(s): |
Loreto Gesualdo, Bari |
Co-investigator(s): |
L Ricciato, Bari V Pavone, Bari |
Project Period: |
10/2015 - 05/2025 |
ClinicalTrials.gov: |
NCT01613118 |