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Zevra Therapeutics, Inc. (ZVRA)

NASDAQ Healthcare Biotechnology
$11.42 ▲ +0.72%
Market Cap
$675.2M
Sector
Healthcare
Industry
Biotechnology
Beta
0.92
52-Wk Range
7.16-15.035
CEO
Neil F. McFarlane
Country
US
Currency
USD

Zevra Therapeutics, Inc. operates in the Biotechnology industry of the Healthcare sector, headquartered in Boston, MA, US. The stock last traded at $11.42, up 0.72% on the session, giving a market capitalisation of $675.2M. On trailing twelve-month figures it carries a trailing P/E of 11.89, a net margin of 42.8%. Its beta of 0.92 implies it has historically moved less than the broad market.

Valuation & profitability (TTM)
P/E
11.89
Price / Sales
4.96
Price / Book
3.10
EV / EBITDA
7.28
Gross margin
95.0%
Operating margin
28.7%
Net margin
42.8%
Return on equity
Debt / equity
0.01
Current ratio
5.17
Dividend yield
0.0%
Payout ratio
0.0%
Company profile
Exchange
NASDAQ Global Select
Employees
61
IPO date
2015-04-16
Headquarters
Boston, MA, US
About Zevra Therapeutics, Inc.

Zevra Therapeutics, Inc., founded in 2006 and based in Celebration, Florida, is a biopharmaceutical company dedicated to discovering and developing innovative treatments for rare diseases. The company employs its proprietary Ligand Activated Therapy (LAT) technology to create novel prodrug versions of existing FDA-approved medications or to enable new applications for other compounds, primarily addressing serious medical conditions within the United States. Zevra's development pipeline is strategically concentrated on high-unmet-need therapeutic areas, including attention deficit hyperactivity disorder (ADHD), stimulant use disorder, and various rare central nervous system (CNS) conditions, such as idiopathic hypersomnia (IH). Their lead product candidate, KP1077, which is a prodrug of d-methylphenidate (known as serdexmethylphenidate), is currently in Phase II clinical trials for the treatment of both IH and narcolepsy. Another key prodrug candidate, KP879, is also advancing through Phase II studies for stimulant use disorder. In addition to its pipeline, Zevra has successfully secured FDA approval for two products: AZSTARYS, a once-daily treatment for ADHD in patients aged six years and older, and APADAZ, an immediate-release combination product containing benzhydrocodone (a prodrug of hydrocodone) and acetaminophen. The company's product portfolio also includes arimoclomol, and it holds collaboration and licensing agreements with KVK-Tech, Inc. and Commave Therapeutics SA. Formerly known as KemPharm, Inc., the company officially rebranded to Zevra Therapeutics, Inc. in February 2023.

Comparable companies

Zevra Therapeutics, Inc. is most often compared with the following Healthcare names:

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