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-0.000365497076023449 0.00146198830409354 -0.000365497076023449 -0.00219298245614043 0.00109649122807009 0.0084064327485379 0.00694444444444436 0.0116959064327484
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Renalys Pharma Reaches Japan PMDA Agreement on Phase III Clinical Trials of Sparsentan for Focal Segmental Glomerulosclerosis (FSGS) and Alport Syndrome (AS) [Yahoo! Finance]

Travere Therapeutics, Inc. (TVTX) 
Company Research Source: Yahoo! Finance
with the Pharmaceuticals and Medical Devices Agency (PMDA) of Japan regarding development plans for two Phase III clinical trials of sparsentan in Japan (development code: RE-021) — one investigating the use of sparsentan in focal segmental glomerulosclerosis (FSGS) and the other in Alport syndrome (AS) in Japan. Both studies are planned as multicenter, open-label, non-controlled Phase III clinical trials involving a small number of patients. Preparations are currently underway for the submission of Clinical Trial Notifications to the PMDA. Renalys remains committed to delivering sparsentan as quickly as possible to patients in Japan and across Asia, with the goal of improving the lives of individuals affected by kidney diseases through the development of innovative therapeutic options. About sparsentan Sparsentan is an oral dual endothelin and angiotensin II receptor antagonist developed by Travere Therapeutics, Inc. ("Travere"). Renalys has an exclusive license for developme Show less Read more
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