Breakdown | |||||
TTM | Dec 2023 | Dec 2022 | Dec 2021 | Dec 2020 | Dec 2019 |
---|---|---|---|---|---|
Income Statement | Total Revenue | ||||
361.10K | 10.00M | 1.51M | 36.46M | 393.00K | -122.00K | Gross Profit |
-387.95K | 7.43M | 571.00K | 18.56M | -15.95M | -23.73M | EBIT |
-37.78M | -28.42M | -43.57M | -20.94M | -37.57M | -39.52M | EBITDA |
-42.27M | -26.06M | -42.06M | -5.00M | -37.52M | -37.56M | Net Income Common Stockholders |
-42.25M | -29.47M | -34.20M | 12.72M | -163.63M | -34.84M |
Balance Sheet | Cash, Cash Equivalents and Short-Term Investments | ||||
56.33M | 57.42M | 56.33M | 94.30M | 23.47M | 16.35M | Total Assets |
88.08M | 66.50M | 88.08M | 126.42M | 62.95M | 86.45M | Total Debt |
12.77M | 5.95M | 12.77M | 16.76M | 17.94M | 32.42M | Net Debt |
-43.56M | -51.47M | -43.56M | -77.54M | -5.53M | 16.07M | Total Liabilities |
26.21M | 15.96M | 26.21M | 38.41M | 77.92M | 46.19M | Stockholders Equity |
61.87M | 50.54M | 61.87M | 88.00M | -14.97M | 40.26M |
Cash Flow | Free Cash Flow | ||||
-25.81M | -21.55M | -38.83M | -5.77M | -28.36M | -45.95M | Operating Cash Flow |
-25.53M | -21.13M | -38.82M | -5.24M | -28.34M | -45.93M | Investing Cash Flow |
-991.53K | -419.00K | 1.50M | -421.00K | 1.50M | 43.30M | Financing Cash Flow |
50.76M | 7.97M | -784.00K | 77.65M | 34.74M | -5.71M |
Name | Overall Rating | Market Cap | P/E Ratio | ROE | Dividend Yield | Revenue Growth | EPS Growth |
---|---|---|---|---|---|---|---|
60 Neutral | $1.18B | ― | -23.01% | ― | 168.06% | 44.66% | |
57 Neutral | $581.14M | ― | -182.71% | ― | 432.03% | 14.41% | |
49 Neutral | $6.85B | 0.81 | -52.91% | 2.50% | 17.48% | 1.17% | |
46 Neutral | $356.83M | ― | -58.31% | ― | ― | ― | |
44 Neutral | $23.55M | ― | -270.01% | ― | -65.96% | 40.80% | |
42 Neutral | $2.88B | ― | -17.90% | ― | ― | -10.27% |
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.