MARKET

TVTX

TVTX

Travere Therapeutics Inc
NASDAQ
5.26
-0.13
-2.41%
After Hours: 5.38 +0.12 +2.28% 16:30 04/26 EDT
OPEN
5.40
PREV CLOSE
5.39
HIGH
5.56
LOW
5.21
VOLUME
1.22M
TURNOVER
0
52 WEEK HIGH
22.75
52 WEEK LOW
5.12
MARKET CAP
400.33M
P/E (TTM)
-3.5067
1D
5D
1M
3M
1Y
5Y
Travere Therapeutics (TVTX) Receives a Hold from Piper Sandler
TipRanks · 14h ago
Buy Rating Affirmed for Travere Therapeutics Following Filspari’s European Approval and Promising US Prospects
TipRanks · 20h ago
Buy Rating Affirmed for Travere Therapeutics on EU Approval and Promising Revenue Projections
TipRanks · 1d ago
Analysts Conflicted on These Healthcare Names: Travere Therapeutics (TVTX), Humana (HUM) and Merck & Company (MRK)
TipRanks · 1d ago
Travere Therapeutics Price Target Raised to $19.00/Share From $17.00 by HC Wainwright & Co.
Dow Jones · 2d ago
Travere Therapeutics Is Maintained at Buy by HC Wainwright & Co.
Dow Jones · 2d ago
HC Wainwright & Co. Maintains Buy on Travere Therapeutics, Raises Price Target to $19
Benzinga · 2d ago
FILSPARI’s European Approval and Market Potential Bolster Buy Rating for Travere Therapeutics
TipRanks · 2d ago
More
About TVTX
Travere Therapeutics, Inc. is a biopharmaceutical company. The Company is focused on identifying, developing, and delivering life-changing therapies to people living with rare kidney and metabolic diseases. Its product, FILSPARI (sparsentan), is indicated to reduce proteinuria in adults with primary IgAN at risk of rapid disease progression. Sparsentan is also in late-stage development for focal segmental glomerulosclerosis (FSGS). The Company’s Pegtibatinase is a novel investigational human enzyme replacement candidate being evaluated for the treatment of classical homocystinuria (HCU), which is a rare metabolic disorder. Its commercial products, Thiola and Thiola EC are for the treatment of cystinuria, a rare genetic cystine transport disorder that causes high cystine levels in the urine and the formation of recurring kidney stones. It is also engaged in the identification of potential small molecule therapeutics for Alagille syndrome (ALGS).

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