Eton Pharmaceuticals, Inc.
NASDAQ•ETON
CEO: Mr. Sean E. Brynjelsen
Sector: Healthcare
Industry: Biotechnology
Listing Date: 2018-11-13
Eton Pharmaceuticals, Inc., a specialty pharmaceutical company, focuses on developing, acquiring, and commercializing pharmaceutical products for rare diseases. The company offers ALKINDI SPRINKLE, a replacement therapy for adrenocortical insufficiency in children under 17 years of age; Carglumic Acid for the treatment of acute and chronic hyperammonemia due to N-acetylglutamate Synthase deficiency; Betaine Anhydrous for the treatment of homocystinuria; and Nitisinone for the treatment of tyrosinemia type 1. It also provides Zeneo hydrocortisone autoinjector for the treatment of adrenal crisis. Eton Pharmaceuticals, Inc. was incorporated in 2017 and is based in Deer Park, Illinois.
Contact Information
21925 W. Field Parkway, Suite 235, Deer Park, IL, 60010-7278, United States
847-787-7361
Market Cap
$810.62M
P/E (TTM)
-173.8
22.2
Dividend Yield
--
52W High
$32.31
52W Low
$13.09
52W Range
Rank56Top 81.7%
2.5
F-Score
Modified Piotroski Analysis
Based on 8-year fundamentals
Weak • 2.5 / 9 points
Scoring Range (0-9)
8-9: Excellent Value
6-7: Strong Fundamentals
4-5: Average Quality
0-3: Weak Performance
Data Period: 2018-2025
Financial Dashboard
Q4 2025 Data
Revenue
$21.28M+0.00%
4-Quarter Trend
EPS
$0.06+0.00%
4-Quarter Trend
FCF
-$22.12M+0.00%
4-Quarter Trend
2025 Annual Earnings Highlights
Key Highlights
Strong Revenue and Profit Growth Total net revenues reached $79.95M USD in 2025, marking a 104.9% increase over $39.01M USD in 2024.
Product Sales Significantly Increased Product sales and royalties totaled $76.7M USD in 2025, driven by INCRELEX®, ALKINDI SPRINKLE®, and GALZIN® volume growth.
Positive Operating Cash Flow Net cash from operations was $10.52M USD in 2025, a substantial improvement from $0.97M USD reported in 2024.
Key Pipeline Progress Noted ET-600 NDA accepted with PDUFA date set for February 25, 2026, anticipating commercial launch shortly thereafter.
Risk Factors
Regulatory Pricing Reforms Impact Inflation Reduction Act reforms may adversely affect realized product prices and demand over time; outcomes remain uncertain.
Reimbursement Constraints Limit Revenue Third-party payor coverage limitations, formulary controls, and utilization management may constrain future net revenues.
Regulatory Approval Uncertainty Product candidates face risks regarding timely FDA approval; ET-700 requires a 2026 PET study for pivotal trials.
Intellectual Property Litigation Risk Dependence on acquired IP rights subjects the company to potential patent infringement lawsuits and associated costs.
Outlook
Advance Pipeline Candidates Plan to advance five late-stage candidates including ET-600, Amglidia®, ET-700, ET-800, and ZENEO® autoinjector.
ET-600 Commercial Launch Scheduled production for ET-600 launch inventory in Q1 2026, following anticipated FDA approval in February 2026.
ET-700 Clinical Trial Execution Scheduled to begin ET-700 proof-of-concept PET study during 2026 to support pivotal clinical trial initiation.
Maintain Commercial Operations Continue leveraging established sales force to commercialize eight existing rare disease products effectively in the U.S.
Peer Comparison
Revenue (TTM)
$299.77M
$79.95M
$79.18M
Gross Margin (Latest Quarter)
100.0%
100.0%
99.5%
Key Metrics
Symbol | Market Cap | P/E (TTM) | ROE (TTM) | Debt to Assets |
|---|---|---|---|---|
| ALMS | $2.90B | -10.1 | -72.7% | 9.0% |
| CRVS | $1.34B | -32.5 | -38.9% | 0.3% |
| LXRX | $1.07B | -37.0 | -18.6% | 21.5% |
Long-Term Trends
Last 4 Quarters
Revenue
Net Income
Operating Cash Flow
4Q Revenue CAGR
7.2%
Steady Growth
4Q Net Income CAGR
N/M
Profitability Shift
Cash Flow Stability
75%
Volatile Cash Flow
Deep Research
Next earnings:May 14, 2026
EPS:$0.10
|Revenue:$22.31M
Financials
Earnings Calls
Reports
News
Income Statement
Balance Sheet
Cash Flow Statement
Ratios
% Chg.
Income Statement | LTM |
|---|
No Data