Breakdown | ||||
Dec 2024 | Dec 2023 | Dec 2022 | Dec 2021 | Dec 2020 |
---|---|---|---|---|
Income Statement | Total Revenue | |||
0.00 | 0.00 | 0.00 | 0.00 | 0.00 | Gross Profit |
0.00 | 0.00 | 0.00 | 0.00 | 0.00 | EBIT |
-111.56M | -83.03M | -53.50M | -194.98M | -37.44M | EBITDA |
-111.56M | -83.03M | -53.50M | -194.98M | -37.44M | Net Income Common Stockholders |
-94.26M | -72.89M | -50.16M | -30.17M | -37.06M |
Balance Sheet | Cash, Cash Equivalents and Short-Term Investments | |||
328.13M | 246.53M | 226.44M | 125.51M | 44.93M | Total Assets |
342.36M | 254.67M | 230.63M | 127.51M | 47.46M | Total Debt |
5.35M | 329.00K | 939.00K | 365.00K | 1.05M | Net Debt |
-54.47M | -175.20M | -19.59M | -86.14M | -23.88M | Total Liabilities |
23.10M | 11.55M | 9.42M | 5.20M | 6.79M | Stockholders Equity |
319.26M | 243.12M | 221.22M | 122.31M | 40.67M |
Cash Flow | Free Cash Flow | |||
-81.54M | -68.47M | -43.62M | -30.17M | -32.52M | Operating Cash Flow |
-81.21M | -68.44M | -43.53M | -30.15M | -32.48M | Investing Cash Flow |
-191.86M | 135.05M | -167.13M | -12.55M | 6.30M | Financing Cash Flow |
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 |
---|---|---|---|---|---|---|---|
60 Neutral | $234.39M | ― | -36.07% | ― | ― | -7.93% | |
52 Neutral | $269.30M | ― | -68.21% | ― | -97.15% | 54.85% | |
50 Neutral | $5.52B | 2.98 | -43.78% | 2.78% | 16.94% | 3.55% | |
46 Neutral | $251.44M | ― | -33.88% | ― | ― | -22.66% | |
41 Neutral | $244.21M | ― | -139.56% | ― | ― | -33.79% | |
39 Underperform | $238.15M | ― | -33.52% | ― | ― | 27.92% | |
38 Underperform | $231.13M | ― | 239.90% | ― | ― | -17.92% |
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.