Breakdown | TTM | Dec 2024 | Dec 2023 | Dec 2022 | Dec 2021 | Dec 2020 |
---|---|---|---|---|---|---|
Income Statement | ||||||
Total Revenue | 1.08B | 682.16M | 556.38M | 1.60B | 1.15B | 475.60M |
Gross Profit | 953.09M | 479.42M | 212.61M | 696.31M | 1.13B | -271.43M |
EBITDA | 495.57M | -108.04M | -487.39M | -604.71M | -1.68B | -398.23M |
Net Income | 422.82M | -187.50M | -545.06M | -657.94M | -1.74B | -427.50M |
Balance Sheet | ||||||
Total Assets | 1.34B | 1.56B | 1.80B | 2.26B | 2.58B | 1.58B |
Cash, Cash Equivalents and Short-Term Investments | 623.05M | 923.12M | 568.50M | 1.34B | 1.52B | 711.05M |
Total Debt | 228.49M | 230.42M | 229.08M | 549.78M | 453.99M | 322.04M |
Total Liabilities | 1.30B | 2.18B | 2.51B | 2.89B | 2.93B | 955.27M |
Stockholders Equity | 37.63M | -623.84M | -716.93M | -634.08M | -351.67M | 627.21M |
Cash Flow | ||||||
Free Cash Flow | -635.41M | -100.32M | -772.77M | -508.92M | 265.46M | -97.16M |
Operating Cash Flow | -630.94M | -87.26M | -713.97M | -415.94M | 322.95M | -42.54M |
Investing Cash Flow | 213.70M | -204.04M | -58.81M | -92.98M | 100.15M | -377.78M |
Financing Cash Flow | -11.62M | 260.58M | 4.47M | 324.99M | 461.71M | 984.76M |
Name | Overall Rating | Market Cap | P/E Ratio | ROE | Dividend Yield | Revenue Growth | EPS Growth |
---|---|---|---|---|---|---|---|
74 Outperform | $1.22B | 5.95 | 34.46% | ― | 799.36% | ― | |
63 Neutral | $1.64B | ― | -5.38% | ― | 26.90% | 62.72% | |
62 Neutral | $818.57M | ― | -43.63% | ― | ― | -13.05% | |
55 Neutral | $1.22B | 3.32 | 30.06% | ― | 9.22% | ― | |
54 Neutral | $1.31B | ― | -15.64% | ― | -0.54% | -6.28% | |
51 Neutral | $7.83B | -0.18 | -40.10% | 2.29% | 21.46% | -2.03% | |
42 Neutral | $1.54B | ― | -63.96% | ― | ― | -36.92% |
On August 27, 2025, Novavax announced that the FDA approved its Nuvaxovid 2025-2026 formula, a protein-based COVID-19 vaccine, for adults 65 and older and individuals 12-64 with underlying conditions. The approval includes extending the vaccine’s shelf life to six months and requires postmarketing studies to assess safety and post-vaccination syndrome. This approval positions Novavax as the only provider of a non-mRNA COVID-19 vaccine in the U.S. for the 2025-2026 season, potentially impacting its market presence and stakeholder interests.
On August 27, 2025, Novavax, Inc. completed a series of privately negotiated exchange and subscription transactions, issuing $225 million in Convertible Senior Notes due 2031. This financial maneuver involved exchanging existing notes and issuing new ones for cash, with the aim of optimizing the company’s capital structure. The notes, which are senior unsecured obligations, offer a conversion option into common stock, potentially affecting the company’s stock issuance and market dynamics. These transactions reflect Novavax’s strategic financial management efforts to enhance its liquidity and operational flexibility.
On August 20, 2025, Novavax announced it had entered into agreements to issue $225 million in 4.625% Convertible Senior Notes due 2031, replacing existing 5.00% Convertible Senior Notes due 2027 and raising new capital. This refinancing extends the maturity of most of its existing debt, improving the company’s capital structure and potentially impacting the market price of its stock and notes. The transactions are expected to close on or about August 27, 2025, with the company planning to use the proceeds for general corporate purposes.
On June 20, 2025, Novavax, Inc. held its Annual Meeting where stockholders voted on several key proposals. The election of three Class III directors, approval of executive compensation, and ratification of Ernst & Young LLP as the independent auditor were all passed, indicating strong shareholder support for the company’s current management and strategic direction.
On June 11, 2025, Novavax announced promising results from the initial cohort of its Phase 3 trial for the COVID-19-Influenza Combination (CIC) and stand-alone influenza vaccine candidates. Both vaccines demonstrated robust immune responses and were well tolerated, showing potential for further development and partnerships. The trial, involving approximately 2,000 adults aged 65 and older, compared these candidates to licensed vaccines Nuvaxovid and Fluzone HD, with results indicating similar immunogenicity and safety profiles. These findings support Novavax’s strategy to pursue partnering opportunities and advance its vaccine programs.