| Breakdown | TTM | Dec 2024 | Dec 2023 | Dec 2022 | Dec 2021 | Dec 2020 |
|---|---|---|---|---|---|---|
Income Statement | ||||||
| Total Revenue | 192.59B | 661.82M | 607.52M | 667.24M | 579.77M | 520.40M |
| Gross Profit | 173.55B | 583.91M | 523.74M | 580.02M | 504.71M | 467.94M |
| EBITDA | 43.05M | 178.28M | 90.04M | 153.44M | 129.19M | 212.40M |
| Net Income | -19.12M | 73.86M | 1.32M | 60.71M | 53.42M | 126.95M |
Balance Sheet | ||||||
| Total Assets | 1.42T | 1.37B | 1.28B | 1.70B | 1.69B | 1.50B |
| Cash, Cash Equivalents and Short-Term Investments | 281.16B | 453.61M | 254.87M | 461.33M | 339.68M | 422.53M |
| Total Debt | 31.42B | 34.27M | 41.53M | 437.97M | 420.55M | 390.33M |
| Total Liabilities | 370.09B | 332.34M | 356.16M | 816.30M | 873.30M | 759.24M |
| Stockholders Equity | 1.05T | 1.04B | 921.52M | 886.20M | 815.85M | 744.86M |
Cash Flow | ||||||
| Free Cash Flow | 44.19M | 171.23M | 110.53M | 116.41M | 125.08M | 134.95M |
| Operating Cash Flow | 44.41M | 171.95M | 111.08M | 116.83M | 127.13M | 138.40M |
| Investing Cash Flow | 42.78M | -189.87M | 268.73M | -216.66M | -81.91M | -34.70M |
| Financing Cash Flow | 6.49M | 12.19M | -397.88M | -10.48M | -130.42M | 3.56M |
Name | Overall Rating | Market Cap | P/E Ratio | ROE | Dividend Yield | Revenue Growth | EPS Growth |
|---|---|---|---|---|---|---|---|
67 Neutral | $1.18B | 9.07 | 18.32% | ― | 1.37% | -18.10% | |
66 Neutral | $2.01B | ― | -2.82% | ― | 38.68% | -160.14% | |
61 Neutral | $1.85B | ― | -0.32% | ― | 79.88% | 99.60% | |
55 Neutral | $3.20B | ― | -1.86% | ― | 4.54% | -130.59% | |
51 Neutral | $7.86B | -0.30 | -43.30% | 2.27% | 22.53% | -2.21% | |
48 Neutral | $1.47B | 24.11 | ― | ― | 98.37% | ― | |
48 Neutral | $2.78B | ― | -0.65% | 5.55% | -2.55% | 66.00% |
Supernus Pharmaceuticals’ recent earnings call painted a mixed picture for investors. While the company reported strong growth in key products and an optimistic financial outlook, these positives were overshadowed by significant operating losses and supply constraints for Onapgo. Despite these challenges, Supernus remains focused on future growth opportunities.
Supernus Pharmaceuticals, Inc. is a biopharmaceutical company that specializes in developing and commercializing treatments for central nervous system (CNS) diseases. The company has a diverse portfolio that includes approved treatments for conditions such as ADHD, Parkinson’s disease, and epilepsy.
On November 4, 2025, Supernus Pharmaceuticals announced that due to stronger than expected demand for ONAPGO, supplier constraints are impacting the company’s ability to fully meet this demand. As a result, the company is prioritizing care for patients currently on ONAPGO by pausing delivery to new patients. The company is working to build adequate inventory and resume new patient initiations as soon as possible. Additionally, Supernus reported a 52% increase in combined revenues of its four growth products in the third quarter of 2025, driven by an increase in net sales of Qelbree and GOCOVRI, and the addition of sales from ZURZUVAE and ONAPGO. The company also completed the acquisition of Sage Therapeutics, Inc. on July 31, 2025, and increased its full-year 2025 revenue guidance.
The most recent analyst rating on (SUPN) stock is a Buy with a $65.00 price target. To see the full list of analyst forecasts on Supernus Pharmaceuticals stock, see the SUPN Stock Forecast page.
Study Overview: Supernus Pharmaceuticals is conducting a Phase 4 observational study titled ‘Real-World Patient Experiences Using Continuous Subcutaneous Apomorphine Infusion (ONAPGOTM) in the United States.’ The study aims to gather real-world data on the experiences of Parkinson’s disease patients using ONAPGOTM, highlighting its significance in understanding patient outcomes and treatment efficacy in everyday settings.
Study Overview: Supernus Pharmaceuticals is conducting a Phase 4 clinical study titled ‘A Phase 4, Randomized, Double-Blind, Multicenter, Placebo-Controlled, Parallel-Group Study of the Efficacy and Safety of SPN-812 in Preschool-Age Children (4 to 5 Years Old) With Attention-Deficit/Hyperactivity Disorder (ADHD)’. The study aims to evaluate the efficacy and safety of SPN-812 (viloxazine extended release) in treating ADHD in young children, a significant step in addressing this condition in early childhood.
Study Overview: Supernus Pharmaceuticals is conducting a study titled An Open-Label Extension, One-Year, Safety, and Efficacy Study of SPN-817 in Adults With Focal Onset Seizures. The study aims to evaluate the long-term safety and efficacy of SPN-817, a promising treatment for focal onset seizures. This study is significant as it could lead to a new therapeutic option for patients with this condition.
Study Overview: The RENAISSANCE 2 study, officially titled ‘RENAISSANCE 2: a Double-Blind, Randomized, Placebo-Controlled, Multicenter, Parallel-Group Study to Evaluate the Efficacy, Safety, and Tolerability of SPN-817 in Adults with Focal Onset Seizures,’ aims to assess the effectiveness and safety of SPN-817 in treating focal onset seizures in adults. This study is significant as it explores a potential new treatment option for a condition that affects many individuals worldwide.
Supernus Pharmaceuticals’ recent earnings call conveyed a cautiously optimistic sentiment, highlighting robust growth in core products and a strategic acquisition that promises future expansion. However, the positive outlook was tempered by a decline in operating earnings and rising expenses.