Breakdown | ||||
Dec 2024 | Dec 2023 | Dec 2022 | Dec 2021 | Dec 2020 |
---|---|---|---|---|
Income Statement | Total Revenue | |||
2.98M | 0.00 | 0.00 | 0.00 | 5.21M | Gross Profit |
2.98M | -147.91M | 0.00 | 0.00 | 0.00 | EBIT |
-202.47M | -191.29M | -116.54M | -84.47M | -932.00K | EBITDA |
-202.47M | -193.76M | -110.75M | -160.99M | -889.00K | Net Income Common Stockholders |
-195.88M | -198.13M | -121.82M | -165.37M | -3.41M |
Balance Sheet | Cash, Cash Equivalents and Short-Term Investments | |||
185.47M | 121.67M | 293.92M | 269.62M | 53.33M | Total Assets |
297.51M | 193.85M | 360.31M | 301.86M | 54.78M | Total Debt |
40.79M | 13.63M | 28.75M | 10.41M | 17.52K | Net Debt |
-141.68M | -27.94M | -158.88M | -175.01M | -36.96M | Total Liabilities |
144.36M | 60.78M | 360.31M | 62.30M | 21.31M | Stockholders Equity |
153.15M | 133.07M | -293.58M | 239.56M | 33.47M |
Cash Flow | Free Cash Flow | |||
-130.16M | -174.14M | -147.92M | -38.23M | -6.18M | Operating Cash Flow |
-122.86M | -165.41M | -131.83M | -34.08M | -5.54M | Investing Cash Flow |
68.46M | 18.71M | -47.10M | -73.63M | -1.06M | Financing Cash Flow |
195.88M | 655.00K | 181.49M | 269.28M | 34.93M |
Name | Overall Rating | Market Cap | P/E Ratio | ROE | Dividend Yield | Revenue Growth | EPS Growth |
---|---|---|---|---|---|---|---|
51 Neutral | $5.31B | 3.33 | -39.82% | 2.92% | 17.95% | 1.84% | |
46 Neutral | $168.01M | ― | -52.00% | ― | -100.00% | 38.72% | |
43 Neutral | $229.53M | ― | -136.88% | ― | ― | 20.58% | |
39 Underperform | $248.59M | ― | 322.49% | ― | -33.83% | 27.89% | |
39 Underperform | $150.48M | ― | -25.95% | ― | ― | ― | |
38 Underperform | $209.55M | ― | -50.84% | ― | ― | 43.21% | |
33 Underperform | $134.77M | ― | -98.10% | ― | -58.64% | -40.05% |
On March 18, 2025, Prime Medicine, Inc. announced a preclinical program for treating alpha-1 antitrypsin deficiency (AATD) using its universal liver lipid nanoparticle to edit the SERPINA1 gene mutation. Initial in vivo data showed promising results with up to 72% precise correction of the gene in humanized mice, restoring over 95% of serum AAT to normal levels. The company plans to advance the AATD program through lead optimization and aims to file an investigational new drug application by mid-2026, indicating significant progress in its liver franchise and potential impact on treating both lung- and liver-associated diseases.