Breakdown | ||||
Dec 2024 | Dec 2023 | Dec 2022 | Dec 2021 | Dec 2020 |
---|---|---|---|---|
Income Statement | Total Revenue | |||
10.90M | 9.56M | 9.22M | 9.33M | 6.79M | Gross Profit |
10.90M | 7.46M | 7.84M | 8.69M | -30.82M | EBIT |
-378.94M | -235.60M | -178.91M | -118.05M | -44.28M | EBITDA |
-378.94M | -233.50M | -177.53M | -117.41M | -43.77M | Net Income Common Stockholders |
-322.30M | -212.22M | -169.08M | -117.37M | -43.98M |
Balance Sheet | Cash, Cash Equivalents and Short-Term Investments | |||
1.50B | 595.35M | 610.73M | 405.54M | 328.14M | Total Assets |
1.56B | 628.55M | 638.80M | 427.58M | 333.90M | Total Debt |
6.80M | 9.85M | 10.69M | 9.96M | 938.00K | Net Debt |
-213.07M | -175.23M | -329.71M | -395.58M | -327.20M | Total Liabilities |
138.94M | 127.79M | 60.73M | 46.15M | 27.68M | Stockholders Equity |
1.42B | 500.76M | 578.08M | 381.43M | 306.22M |
Cash Flow | Free Cash Flow | |||
-307.94M | -123.29M | -139.09M | -98.55M | -38.21M | Operating Cash Flow |
-300.87M | -119.06M | -136.27M | -94.81M | -37.12M | Investing Cash Flow |
-854.20M | -130.07M | -189.96M | -82.52M | -7.79M | Financing Cash Flow |
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 |
---|---|---|---|---|---|---|---|
69 Neutral | $3.64B | 7.05 | 33.08% | ― | 91.12% | ― | |
55 Neutral | $3.52B | ― | -35.56% | ― | -41.66% | -180.15% | |
54 Neutral | $3.50B | ― | -51.57% | ― | 730.42% | 31.63% | |
53 Neutral | $5.14B | 3.03 | -44.09% | 2.83% | 16.75% | -0.06% | |
52 Neutral | $3.97B | ― | -418.97% | ― | 48.88% | 39.30% | |
52 Neutral | $3.69B | ― | -34.19% | ― | -17.87% | -1.89% | |
43 Neutral | $3.37B | ― | -386.33% | ― | 33.46% | 26.72% |
On March 17, 2025, Avidity Biosciences announced the topline data from its Phase 1/2 EXPLORE44 trial for delpacibart zotadirsen (del-zota) in patients with Duchenne muscular dystrophy amenable to exon 44 skipping. The trial results showed consistent delivery of PMOs to skeletal muscle, increased exon 44 skipping, enhanced dystrophin production, and reduced creatine kinase levels, demonstrating favorable safety and tolerability. The company plans to submit a Biologics License Application by the end of 2025, aiming for accelerated approval in the U.S.