Zevra Therapeutics' MIPLYFFA™ (arimoclomol) Receives U.S. FDA Approval as Treatment for Niemann-Pick Disease Type C [Yahoo! Finance]
Zevra Therapeutics, Inc. (ZVRA)
Company Research
Source: Yahoo! Finance
MIPLYFFA is indicated for use in combination with miglustat for the treatment of neurological manifestations of NPC in adults and pediatric patients 2 years of age and older Zevra receives rare pediatric disease priority review voucher in conjunction with approval Company launches AmplifyAssist™ patient support program Conference call and webcast set for 8:00 a.m. EDT on Monday, Sept. 23, 2024 CELEBRATION, Fla., Sept. 20, 2024 (GLOBE NEWSWIRE) -- Zevra Therapeutics, Inc. (NasdaqGS: ZVRA) (Zevra, or the Company), a commercial-stage rare disease therapeutics company, today announced that the U.S. Food and Drug Administration (FDA) has approved MIPLYFFA™ (MY-PLY-FAH) (arimoclomol) capsules as an orally delivered treatment for Niemann-Pick disease type C (NPC). The first NPC drug approved by the FDA, MIPLYFFA is indicated for use in combination with miglustat for the treatment of neurological manifestations of NPC in adult and pediatric patients 2 years of age and older. In addit
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News
- Zevra Therapeutics to Present at the 21st Annual WORLDSymposium™ [Yahoo! Finance]Yahoo! Finance
- Zevra Therapeutics to Present at the 21st Annual WORLDSymposium™GlobeNewswire
- Zevra Therapeutics, Inc. (NASDAQ: ZVRA) was upgraded by analysts at Cantor Fitzgerald to a "strong-buy" rating.MarketBeat
- Zevra Therapeutics to Participate at Upcoming Investor ConferencesGlobeNewswire
- Zevra Therapeutics, Inc. (NASDAQ: ZVRA) is now covered by analysts at Cantor Fitzgerald. They set an "overweight" rating and a $25.00 price target on the stock.MarketBeat
ZVRA
Earnings
- 11/12/24 - Miss
ZVRA
Sec Filings
- 2/14/25 - Form 4
- 2/14/25 - Form 4
- 2/14/25 - Form 4
- ZVRA's page on the SEC website