Zevra Therapeutics (NASDAQ:ZVRA – Get Free Report) and Cassava Sciences (NASDAQ:FLNA – Get Free Report) are both small-cap medical companies, but which is the better business? We will contrast the two businesses based on the strength of their risk, valuation, dividends, institutional ownership, analyst recommendations, earnings and profitability.
Risk & Volatility
Zevra Therapeutics has a beta of 0.89, suggesting that its stock price is 11% less volatile than the S&P 500. Comparatively, Cassava Sciences has a beta of -0.67, suggesting that its stock price is 167% less volatile than the S&P 500.
Profitability
This table compares Zevra Therapeutics and Cassava Sciences’ net margins, return on equity and return on assets.
| Net Margins | Return on Equity | Return on Assets | |
| Zevra Therapeutics | 78.17% | 57.42% | 26.03% |
| Cassava Sciences | N/A | -59.34% | -42.05% |
Earnings and Valuation
| Gross Revenue | Price/Sales Ratio | Net Income | Earnings Per Share | Price/Earnings Ratio | |
| Zevra Therapeutics | $106.47 million | 5.60 | $83.23 million | $1.33 | 7.58 |
| Cassava Sciences | N/A | N/A | -$90.97 million | ($1.88) | -0.86 |
Zevra Therapeutics has higher revenue and earnings than Cassava Sciences. Cassava Sciences is trading at a lower price-to-earnings ratio than Zevra Therapeutics, indicating that it is currently the more affordable of the two stocks.
Analyst Recommendations
This is a breakdown of recent ratings and target prices for Zevra Therapeutics and Cassava Sciences, as provided by MarketBeat.
| Sell Ratings | Hold Ratings | Buy Ratings | Strong Buy Ratings | Rating Score | |
| Zevra Therapeutics | 0 | 2 | 7 | 0 | 2.78 |
| Cassava Sciences | 1 | 0 | 0 | 0 | 1.00 |
Zevra Therapeutics presently has a consensus target price of $23.00, indicating a potential upside of 128.17%. Given Zevra Therapeutics’ stronger consensus rating and higher probable upside, research analysts clearly believe Zevra Therapeutics is more favorable than Cassava Sciences.
Institutional & Insider Ownership
35.0% of Zevra Therapeutics shares are held by institutional investors. Comparatively, 38.1% of Cassava Sciences shares are held by institutional investors. 2.4% of Zevra Therapeutics shares are held by company insiders. Comparatively, 44.9% of Cassava Sciences shares are held by company insiders. Strong institutional ownership is an indication that large money managers, hedge funds and endowments believe a company is poised for long-term growth.
Summary
Zevra Therapeutics beats Cassava Sciences on 11 of the 13 factors compared between the two stocks.
About Zevra Therapeutics
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.
About Cassava Sciences
Filana Therapeutics Inc is a biotechnology company focused on developing novel, investigational therapies to modulate the filamin A protein for the treatment of central nervous system disorders, such as tuberous sclerosis complex (TSC)-related epilepsy, and other diseases associated with dysregulation or overexpression of filamin A. Its therapeutic product candidate, simufilam, is a proprietary small molecule oral treatment drug being studied for the treatment of TSC-related epilepsy.
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