| Breakdown | TTM | Dec 2024 | Dec 2023 | Dec 2022 | Dec 2021 | Dec 2020 |
|---|---|---|---|---|---|---|
Income Statement | ||||||
| Total Revenue | 706.00K | 0.00 | 0.00 | 0.00 | 0.00 | 0.00 |
| Gross Profit | 706.00K | 0.00 | 0.00 | 0.00 | 0.00 | 0.00 |
| EBITDA | -134.05M | -111.56M | -83.03M | -53.50M | -30.36M | -37.41M |
| Net Income | -124.03M | -94.26M | -72.89M | -51.83M | -194.91M | -37.30M |
Balance Sheet | ||||||
| Total Assets | 271.87M | 342.36M | 254.67M | 230.63M | 127.51M | 47.46M |
| Cash, Cash Equivalents and Short-Term Investments | 227.72M | 328.13M | 246.53M | 226.44M | 125.51M | 44.93M |
| Total Debt | 4.46M | 5.35M | 329.00K | 939.00K | 365.00K | 1.05M |
| Total Liabilities | 38.61M | 23.10M | 11.55M | 9.42M | 5.20M | 6.79M |
| Stockholders Equity | 233.25M | 319.26M | 243.12M | 221.22M | 122.31M | 40.67M |
Cash Flow | ||||||
| Free Cash Flow | -120.32M | -81.54M | -68.47M | -43.62M | -30.17M | -32.52M |
| Operating Cash Flow | -119.73M | -81.21M | -68.44M | -43.53M | -30.15M | -32.48M |
| Investing Cash Flow | 135.11M | -191.86M | 135.05M | -167.13M | -12.55M | 6.30M |
| Financing Cash Flow | 3.00K | 157.20M | 88.40M | 144.72M | 104.28M | 40.86M |
Name | Overall Rating | Market Cap | P/E Ratio | ROE | Dividend Yield | Revenue Growth | EPS Growth |
|---|---|---|---|---|---|---|---|
55 Neutral | $403.97M | 9.39 | 14.55% | ― | 1268.81% | ― | |
53 Neutral | $578.78M | ― | -45.38% | ― | ― | ― | |
52 Neutral | $1.00B | 55.21 | 9.28% | ― | 1112.27% | ― | |
51 Neutral | $7.86B | -0.30 | -43.30% | 2.27% | 22.53% | -2.21% | |
47 Neutral | $356.63M | ― | -60.52% | ― | 407.86% | 30.35% | |
47 Neutral | $569.83M | ― | ― | ― | 6.35% | 39.57% | |
44 Neutral | $719.27M | ― | -43.15% | ― | ― | -2.74% |
Astria Therapeutics has announced the design of the ALPHA-ORBIT Phase 3 clinical trial for navenibart, a treatment for hereditary angioedema, which will feature both every 3- and 6-month treatment arms. This trial aims to support global registration and is expected to initiate in Q1 2025. The company is pioneering flexible dosing options to potentially make navenibart a market-leading choice for HAE therapy, and the trial design incorporates feedback from regulatory authorities and collaboration with patients and physicians.