Theratechnologies Receives FDA Approval for EGRIFTA WR™ (Tesamorelin F8) to Treat Excess Visceral Abdominal Fat in Adults with HIV and Lipodystrophy
Theratechnologies Inc. - Common Shares (THTX)
Company Research
Source: GlobeNewswire
New, improved formulation set to replace EGRIFTA SV® MONTREAL, March 25, 2025 (GLOBE NEWSWIRE) -- Theratechnologies Inc. (“Theratechnologies” or the “Company”) (TSX: TH) (NASDAQ: THTX), a commercial-stage biopharmaceutical company, today announced that the U.S. Food and Drug Administration (FDA) has approved the Company’s supplemental Biologics License Application (sBLA) for the F8 formulation of tesamorelin for injection. The Company will commercialize the new formulation under the tradename EGRIFTA WR™. Tesamorelin for injection is the only medication approved in the U.S. for the reduction of excess abdominal fat in adults with HIV who have lipodystrophy. The new formulation, EGRIFTA WR™, is a daily injectable but
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News
- TSX futures flat as markets await clarity on tariffs [Yahoo! Finance Canada]Yahoo! Finance Canada
- Theratechnologies Presents Encouraging Virologic Suppression Data from the PROMISE-US Trial of Ibalizumab at CROIGlobeNewswire
- Theratechnologies CROI Presentation Highlights Limitations of Using BMI to Assess Cardiovascular (CV) Risk in People with HIVGlobeNewswire
- Theratechnologies Reports Financial Results for the Fourth Quarter and Full Year of Fiscal 2024GlobeNewswire
- Theratechnologies Inc. (NASDAQ: THTX) was upgraded by analysts at Research Capitl to a "strong-buy" rating.MarketBeat
THTX
Analyst Actions
- 2/14/25 - MACKIE RESEARCH
THTX
Sec Filings
- 3/26/25 - Form 6-K
- 2/26/25 - Form 20-F
- 2/26/25 - Form 6-K
- THTX's page on the SEC website