March 17 (Reuters) - Travere Therapeutics Inc TVTX.O:
TRAVERE THERAPEUTICS SUBMITS SNDA TO FDA FOR APPROVAL OF FILSPARI® (SPARSENTAN) FOR THE TREATMENT OF FSGS
TRAVERE THERAPEUTICS INC: FDA NOTIFIED COMPANY THAT REMS MONITORING FOR EMBRYO-FETAL TOXICITY IS NO LONGER NECESSARY
TRAVERE THERAPEUTICS INC: PLANS TO SUBMIT AMENDMENT TO REMS SNDA CURRENTLY UNDER REVIEW FOR MODIFICATION OF LIVER MONITORING
TRAVERE THERAPEUTICS INC: CONTINUES TO EXPECT A REMS MODIFICATION PDUFA TARGET ACTION DATE OF AUGUST 28
Source text: ID:nGNX583jwH
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((Reuters.Briefs@thomsonreuters.com))