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 |
---|---|---|---|---|---|---|---|
51 Neutral | $321.68M | ― | -33.52% | ― | ― | 27.92% | |
49 Neutral | $6.85B | 0.81 | -52.91% | 2.50% | 17.48% | 1.17% | |
46 Neutral | $3.17B | ― | -19.20% | ― | -89.95% | -123.71% | |
41 Neutral | $184.26M | ― | -187.83% | ― | -67.20% | 64.66% | |
41 Neutral | $147.30M | ― | -43.72% | ― | 190.40% | 7.54% | |
39 Underperform | $103.72M | ― | -98.10% | ― | -58.64% | -40.05% | |
39 Underperform | $835.39M | ― | -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.