1180 Celebration Boulevard
Suite 103
Celebration, FL 34747
United States
321 939 3416
https://zevra.com
Sector(s): Healthcare
Industry: Biotechnology
Full-time employees: 65
Name | Title | Pay | Exercised | Year born |
---|---|---|---|---|
Mr. Neil F. McFarlane | President, CEO & Director | 503.77k | N/A | 1973 |
Ms. Christal M. M. Mickle M.A. | Co-Founder & Chief Development Officer | 622.36k | N/A | 1979 |
Mr. R. LaDuane Clifton CPA | CFO, Secretary & Treasurer | 658.43k | N/A | 1972 |
Mr. Joshua M. Schafer M.B.A. | Chief Commercial Officer & Executive VP of Business Development | 766.07k | N/A | 1972 |
Dr. Sven Guenther Ph.D. | Chief Scientific Officer | 497.26k | N/A | 1972 |
Ms. Nichol L. Ochsner | Vice President of Investor Relations & Corporate Communications | N/A | N/A | N/A |
Dr. Christopher M. Lauderback Ph.D. | Senior Vice President of Manufacturing | N/A | N/A | 1975 |
Dr. Rene A. Braeckman Ph.D. | Senior Vice President of Clinical Development | N/A | N/A | N/A |
Dr. Daniel Gallo Ph.D. | Senior Vice President of Medical Affairs & Advocacy | N/A | N/A | N/A |
Dr. Adrian Quartel FFPM, M.D. | Chief Medical Officer | N/A | N/A | 1961 |
Zevra Therapeutics, Inc. discovers and develops various proprietary prodrugs to treat serious medical conditions in the United States. The company develops its products through Ligand Activated Therapy platform. Its lead product candidate is KP1077, consisting of KP1077IH, which is under Phase 2 clinical trial for the treatment of idiopathic hypersomnia, and KP1077N, which is under Phase ½ clinical trial to treat narcolepsy. The company is also developing Celiprolol, a prodrug product candidate that is under Phase 1/2 clinical trial for the treatment of vascular Ehlers Danlos syndrome. In addition, it offers AZSTARYS, a once-daily treatment for attention deficit hyperactivity disorder in patients aged six years and older; OLPRUVA to treat urea cycle disorders; and Arimoclomol for the treatment of niemann pick disease type C, an ultra-rare neurodegenerative lysosomal storage disorder. The company has collaboration and license agreement with Commave Therapeutics SA to develop, manufacture and commercialize the company's product candidates containing SDX and d-methylphenidate; and license agreement with Acer and Relief Therapeutics, Inc. to develop and commercialize rights for OLPRUVA. The company was formerly known as KemPharm, Inc. and changed its name to Zevra Therapeutics, Inc. in February 2023. Zevra Therapeutics, Inc. was incorporated in 2006 and is headquartered in Celebration, Florida.
Zevra Therapeutics, Inc.’s ISS governance QualityScore as of 1 May 2024 is 8. The pillar scores are Audit: 9; Board: 4; Shareholder rights: 8; Compensation: 9.