Breakdown | |||||
TTM | Dec 2023 | Dec 2022 | Dec 2021 | Dec 2020 | Dec 2019 |
---|---|---|---|---|---|
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 | -26.00K | EBIT |
-100.97M | -83.03M | -53.50M | -194.98M | -37.44M | -27.09M | EBITDA |
-116.17M | -83.03M | -53.50M | -194.98M | -37.44M | -26.27M | Net Income Common Stockholders |
-100.04M | -72.89M | -50.16M | -30.17M | -37.06M | -26.24M |
Balance Sheet | Cash, Cash Equivalents and Short-Term Investments | ||||
37.57M | 246.53M | 226.44M | 125.51M | 44.93M | 36.24M | Total Assets |
39.17M | 254.67M | 230.63M | 127.51M | 47.46M | 41.78M | Total Debt |
0.00 | 329.00K | 939.00K | 365.00K | 1.05M | 2.25M | Net Debt |
-15.29M | -175.20M | -19.59M | -86.14M | -23.88M | -7.65M | Total Liabilities |
4.23M | 11.55M | 9.42M | 5.20M | 6.79M | 6.06M | Stockholders Equity |
34.94M | 243.12M | 221.22M | 122.31M | 40.67M | 35.72M |
Cash Flow | Free Cash Flow | ||||
-94.43M | -68.47M | -43.62M | -30.17M | -32.52M | -26.58M | Operating Cash Flow |
-94.09M | -68.44M | -43.53M | -30.15M | -32.48M | -26.57M | Investing Cash Flow |
-190.16M | 135.05M | -167.13M | -12.55M | 6.30M | -4.08M | Financing Cash Flow |
245.18M | 88.40M | 144.72M | 104.28M | 40.86M | 25.62M |
Name | Overall Rating | Market Cap | P/E Ratio | ROE | Dividend Yield | Revenue Growth | EPS Growth |
---|---|---|---|---|---|---|---|
51 Neutral | $365.13M | ― | -38.03% | ― | ― | 4.90% | |
49 Neutral | $6.84B | 0.05 | -53.14% | 2.48% | 24.49% | -3.26% | |
47 Neutral | $190.93M | ― | -67.62% | ― | 346.02% | 28.96% | |
46 Neutral | $3.63B | ― | -19.20% | ― | -89.95% | -123.71% | |
42 Neutral | $206.96M | ― | -156.42% | ― | -74.04% | 48.16% | |
39 Underperform | $125.29M | ― | -98.10% | ― | -58.64% | -40.05% | |
39 Underperform | $962.71M | ― | -54.00% | ― | 59.55% | 3.09% |
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.
Astria Therapeutics, Inc. has amended its 2022 Inducement Stock Incentive Plan to increase the shares of common stock reserved for issuance from 1,700,000 to 2,800,000. This amendment, made without stockholder approval, aims to attract new talent by offering stock awards to individuals not previously employed by the company, potentially strengthening its workforce and aligning employee interests with those of shareholders.