| Breakdown | TTM | Dec 2024 | Dec 2023 | Dec 2022 | Dec 2021 | Dec 2020 |
|---|---|---|---|---|---|---|
Income Statement | ||||||
| Total Revenue | 20.87M | 10.90M | 9.56M | 9.22M | 9.33M | 6.79M |
| Gross Profit | -117.26M | 10.90M | 7.46M | 7.84M | -91.86M | -30.82M |
| EBITDA | -594.70M | -376.16M | -233.50M | -177.53M | -117.41M | -43.77M |
| Net Income | -549.79M | -322.30M | -212.22M | -174.00M | -118.01M | -44.35M |
Balance Sheet | ||||||
| Total Assets | 2.13B | 1.56B | 628.55M | 638.80M | 427.58M | 333.90M |
| Cash, Cash Equivalents and Short-Term Investments | 1.88B | 1.50B | 595.35M | 610.73M | 405.54M | 328.14M |
| Total Debt | 49.97M | 6.80M | 9.85M | 10.69M | 11.73M | 938.00K |
| Total Liabilities | 247.94M | 138.94M | 127.79M | 60.73M | 46.15M | 27.68M |
| Stockholders Equity | 1.89B | 1.42B | 500.76M | 578.08M | 381.43M | 306.22M |
Cash Flow | ||||||
| Free Cash Flow | -595.44M | -307.94M | -123.29M | -139.09M | -98.55M | -38.21M |
| Operating Cash Flow | -580.54M | -300.87M | -119.06M | -136.27M | -94.81M | -37.12M |
| Investing Cash Flow | -309.43M | -854.20M | -130.07M | -189.96M | -82.52M | -7.79M |
| Financing Cash Flow | 869.80M | 1.19B | 93.86M | 346.17M | 176.32M | 272.04M |
Name | Overall Rating | Market Cap | P/E Ratio | ROE | Dividend Yield | Revenue Growth | EPS Growth |
|---|---|---|---|---|---|---|---|
72 Outperform | $6.31B | 9.22 | ― | ― | 97.54% | ― | |
62 Neutral | $10.91B | -17.31 | -32.44% | ― | 106.27% | -43.90% | |
59 Neutral | $7.48B | -36.38 | -240.36% | ― | 54.92% | 28.47% | |
52 Neutral | $7.36B | -18.17 | -51.57% | ― | 57.54% | -36.57% | |
51 Neutral | $7.86B | -0.30 | -43.30% | 2.27% | 22.53% | -2.21% | |
45 Neutral | $5.38B | -9.73 | -95.93% | ― | ― | -27.70% | |
40 Underperform | $5.32B | -10.38 | -25.33% | ― | -81.10% | -99.21% |
On October 25, 2025, Avidity Biosciences entered into a merger agreement under which a Novartis wholly owned subsidiary will merge with Avidity, leaving Avidity as an indirect wholly owned subsidiary of Novartis, and on December 14, 2025 the board approved steps to manage tax and compensation consequences tied to that deal. To mitigate potential “excess parachute payment” consequences under Sections 280G and 4999 of the U.S. tax code and preserve corporate tax deductions, the board accelerated into December 2025 the vesting and payment of certain 2025 bonuses and performance stock units that would otherwise have been paid on closing of the merger or in 2026 for selected executives, including specified cash bonuses and large tranches of performance stock units for four named officers, with no duplication of compensation and subject to tax withholding. Each affected executive entered into a clawback agreement requiring repayment of the accelerated amounts if they are terminated for cause or resign without good reason before the date those payments would originally have been made (or, for accelerated PSUs, before December 31, 2029). Separately, following Hart-Scott-Rodino filings on November 21, 2025, the Federal Trade Commission on December 17, 2025 granted early termination of the HSR waiting period for the merger and related spin-off transactions, clearing a key antitrust condition, though completion of the deal still depends on the separation of Atrium Therapeutics (SpinCo) and other customary closing conditions.
On October 25, 2025, Avidity Biosciences announced a merger agreement with Novartis AG, under which Novartis will acquire Avidity for $72.00 per share, valuing the company at approximately $12 billion. The merger includes the separation of Avidity’s early-stage precision cardiology programs into a new entity, SpinCo, which will be led by Kathleen Gallagher. The acquisition will provide Novartis with access to Avidity’s RNA-targeting delivery platform and its late-stage clinical programs. The transaction, expected to close in the first half of 2026, requires regulatory and stockholder approvals and is anticipated to enhance Novartis’ neuroscience pipeline.
On October 13, 2025, Avidity Biosciences announced a delay in the submission of its Biologics License Application for del-zota to the first quarter of 2026, following a pre-BLA meeting with the FDA. This delay is intended to provide additional non-clinical data to support the chemistry, manufacturing, and controls package, impacting the company’s timeline for regulatory approval.