Breakdown | TTM | Dec 2024 | Dec 2023 | Dec 2022 | Dec 2021 | Dec 2020 |
---|---|---|---|---|---|---|
Income Statement | ||||||
Total Revenue | 0.00 | 0.00 | 0.00 | 0.00 | 0.00 | 0.00 |
Gross Profit | 0.00 | 0.00 | 0.00 | 0.00 | 0.00 | 0.00 |
EBITDA | -131.42M | -94.26M | -83.03M | -53.50M | -194.98M | -37.44M |
Net Income | -116.92M | -94.26M | -72.89M | -51.83M | -194.91M | -37.30M |
Balance Sheet | ||||||
Total Assets | 281.92M | 342.36M | 254.67M | 230.63M | 127.51M | 47.46M |
Cash, Cash Equivalents and Short-Term Investments | 259.18M | 328.13M | 246.53M | 226.44M | 125.51M | 44.93M |
Total Debt | 4.77M | 5.35M | 329.00K | 939.00K | 365.00K | 1.05M |
Total Liabilities | 21.41M | 23.10M | 11.55M | 9.42M | 5.20M | 6.79M |
Stockholders Equity | 260.51M | 319.26M | 243.12M | 221.22M | 122.31M | 40.67M |
Cash Flow | ||||||
Free Cash Flow | -116.01M | -81.54M | -68.47M | -43.62M | -30.17M | -32.52M |
Operating Cash Flow | -115.40M | -81.21M | -68.44M | -43.53M | -30.15M | -32.48M |
Investing Cash Flow | 89.05M | -191.86M | 135.05M | -167.13M | -12.55M | 6.30M |
Financing Cash Flow | 15.30M | 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 |
---|---|---|---|---|---|---|---|
61 Neutral | $421.46M | 9.97 | 14.55% | ― | 1268.81% | ― | |
54 Neutral | $441.79M | ― | -52.18% | ― | 187.52% | 26.32% | |
54 Neutral | $497.25M | ― | 123.38% | ― | 15.73% | 38.73% | |
52 Neutral | $415.65M | ― | -38.87% | ― | ― | ― | |
52 Neutral | $620.06M | 29.26 | 9.81% | ― | 2990.57% | ― | |
51 Neutral | $7.86B | -0.30 | -43.30% | 2.27% | 22.53% | -2.21% | |
44 Neutral | $468.97M | ― | -38.49% | ― | ― | 11.81% |
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.