Breakdown | TTM | Dec 2024 | Dec 2023 | Dec 2022 | Dec 2021 | Dec 2020 |
---|---|---|---|---|---|---|
Income Statement | ||||||
Total Revenue | 1.56M | 0.00 | 10.00M | 1.51M | 36.46M | 393.00K |
Gross Profit | 344.20K | -1.09M | 7.43M | 571.00K | 18.56M | -15.95M |
EBITDA | -46.77M | -42.46M | -26.06M | -42.06M | -5.00M | -37.52M |
Net Income | -49.55M | -43.25M | -29.47M | -34.20M | 12.72M | -163.63M |
Balance Sheet | ||||||
Total Assets | 62.63M | 76.39M | 66.50M | 88.08M | 126.42M | 62.95M |
Cash, Cash Equivalents and Short-Term Investments | 56.13M | 69.80M | 57.42M | 56.33M | 94.30M | 23.47M |
Total Debt | 601.00K | 6.43M | 5.95M | 12.77M | 16.76M | 17.94M |
Total Liabilities | 8.45M | 15.42M | 15.96M | 26.21M | 38.41M | 77.92M |
Stockholders Equity | 54.18M | 60.97M | 50.54M | 61.87M | 88.00M | -14.97M |
Cash Flow | ||||||
Free Cash Flow | -32.94M | -33.53M | -21.55M | -38.83M | -5.77M | -28.36M |
Operating Cash Flow | -32.92M | -32.83M | -21.13M | -38.82M | -5.24M | -28.34M |
Investing Cash Flow | -322.14K | -699.00K | -419.00K | 1.50M | -421.00K | 1.50M |
Financing Cash Flow | -346.00K | 46.15M | 7.97M | -784.00K | 77.65M | 34.74M |
Name | Overall Rating | Market Cap | P/E Ratio | ROE | Dividend Yield | Revenue Growth | EPS Growth |
---|---|---|---|---|---|---|---|
59 Neutral | $497.57M | -2.79 | -82.17% | ― | 74.95% | 34.25% | |
53 Neutral | $805.86M | -1.42 | 172.73% | ― | -12.52% | -82.84% | |
52 Neutral | $992.16M | -5.28 | -40.27% | ― | 271.44% | 26.65% | |
48 Neutral | $232.81M | -127.27 | 3.42% | ― | 9.78% | 98.13% | |
43 Neutral | $311.64M | ― | -75.08% | ― | ― | ― | |
39 Underperform | $256.12M | -0.19 | 1138.25% | ― | ― | ― | |
51 Neutral | $7.86B | -0.30 | -43.30% | 2.27% | 22.53% | -2.21% |
Mereo BioPharma has announced updates on its lead clinical programs, including the ongoing Phase 3 study of setrusumab for osteogenesis imperfecta and the positive EMA opinion on alvelestat for alpha-1 antitrypsin deficiency-associated lung disease. The company is confident in the potential of setrusumab to become the standard-of-care and is prepared for key milestones through 2027, leveraging its cash runway and strategic partnerships. The Orphan Designation for alvelestat is a significant step towards its commercialization in Europe, promising benefits for patients with rare conditions.