Zevra Stock Surges Close to 70% in 3 Months: Here's Why [Yahoo! Finance]
Zevra Therapeutics, Inc. (ZVRA)
Company Research
Source: Yahoo! Finance
ZVRA obtained FDA approval for arimoclomol capsules for the treatment of Niemann-Pick disease type C (NPC) in September. The drug will be marketed under the brand name Miplyffa. The FDA approved Miplyffa for use in combination with miglustat for the treatment of neurological manifestations of NPC in adult and pediatric patients aged two years and above. Following the FDA nod, Miplyffa became the first treatment to be approved for NPC, an ultra-rare and progressive neurodegenerative disease. Additionally, Zevra received a rare pediatric disease priority review voucher in conjunction with the FDA approval for Miplyffa. Shares of Zevra have surged 68.5% in the past three months compared with the industry's rise of 9.3%. Image Source: Zacks Investment Research The FDA approval for Miplyffa can be attributed as the reason for the stock price rally as the drug became the first approved treatment for this rare and devastating disease. NPC is an ultra-rare, progressive, and neur
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ZVRA
News
- Zevra Therapeutics to be Added to Nasdaq Biotechnology Index (Nasdaq: NBI) Effective December 23, 2024 [Yahoo! Finance]Yahoo! Finance
- Zevra Therapeutics to be Added to Nasdaq Biotechnology Index (Nasdaq: NBI) Effective December 23, 2024GlobeNewswire
- Zevra Therapeutics Announces Organizational ChangesGlobeNewswire
- Zevra Therapeutics to Participate at Upcoming Investor ConferencesGlobeNewswire
- Zevra Therapeutics Announces U.S. Commercial Availability of MIPLYFFA™ (arimoclomol) for Treatment of Niemann-Pick Disease Type CGlobeNewswire
ZVRA
Earnings
- 11/12/24 - Miss
ZVRA
Sec Filings
- 12/6/24 - Form 8-K
- 11/22/24 - Form 8-K
- 11/14/24 - Form SCHEDULE
- ZVRA's page on the SEC website