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ZEVRA THERAPEUTICS INC

ZVRANASDAQ
πŸ† #2554 by market capEarnings Nov 4US Equity
$11.42β–² $0.08 (+0.66%)
Live
1hβ–Ό 0.5%
24hβ–² 0.7%
7dβ–² 8.3%
14dβ–² 16.7%
30dβ–Ό 13.4%
1yβ–Ό 3.0%
🏦Market Cap
$675M
Small Cap
πŸ“ˆRevenue Growth (YoY)
+350.9%
High Growth
πŸ“ŠGross Margin
95.0%
High
πŸ’΅FCF Margin
24.0%
Strong
βš–οΈP/S Ratio
5.0x
Fair
Otter Score
59
Weak

Trading Snapshot

Day Range
$11.37 – $11.55
52-Week Range
$7.16 – $15.04
Volume
$2.60B
Avg Volume
$1.90B
Shares Outstanding
59.1M
Next Earnings
Oct 25, 2026

Fundamentals Snapshot

Annual Revenue
$106M
Last Q Revenue
$40M
P/E Ratio
11.9
P/S Ratio
5.0x
EPS (TTM)
$0.98
Dividend Yield
0.00%

Why Investors Own ZVRA

  • βœ“High-growth profile β€” revenue up +46.1% YoY with expanding US Equity exposure.
  • βœ“Healthy economics β€” 80% gross margin and 16% free-cash-flow margin.
  • βœ“New products and segments could unlock additional revenue streams.
⚠️ Key Risks

Execution delays, intensifying competition, and valuation compression if growth decelerates.

Financial Trends

Revenue (TTM)
$106Mβ–² +49.1% YoY
Gross Margin (TTM)
79.9%β–² +2.2% YoY
Operating Income (TTM)
$29Mβ–² +49.1% YoY
Free Cash Flow (TTM)
$17Mβ–² +49.1% YoY

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.

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Otter Score Breakdown

β“˜
πŸ’ŽQualityβ˜…β˜…β˜…β˜…β˜…
πŸš€Growthβ˜…β˜…β˜…β˜…β˜…
βš–οΈValuationβ˜…β˜…β˜…β˜…β˜…
⚑Momentumβ˜…β˜…β˜…β˜…β˜…
Overall Score
Weak
59/100

Analyst Price Target

β“˜
Average Target
$15.28
β–² +33.8% Upside
High Target$18.17
Low Target$12.10
Based on 22 analysts

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