| Breakdown | TTM | Dec 2024 | Dec 2023 | Dec 2022 | Dec 2021 | Dec 2020 |
|---|---|---|---|---|---|---|
Income Statement | ||||||
| Total Revenue | 5.98M | 2.98M | 0.00 | 0.00 | 0.00 | 5.21M |
| Gross Profit | -39.88M | 2.98M | 0.00 | 0.00 | 0.00 | 2.23M |
| EBITDA | -193.41M | -196.34M | -186.64M | -114.32M | -83.91M | -889.00K |
| Net Income | -197.34M | -195.88M | -198.13M | -121.82M | -165.37M | -3.41M |
Balance Sheet | ||||||
| Total Assets | 385.01M | 297.51M | 193.85M | 360.31M | 301.86M | 54.78M |
| Cash, Cash Equivalents and Short-Term Investments | 208.43M | 190.44M | 121.67M | 293.92M | 269.62M | 53.33M |
| Total Debt | 118.14M | 40.79M | 13.63M | 28.75M | 10.41M | 0.00 |
| Total Liabilities | 223.19M | 144.36M | 60.78M | 44.04M | 62.30M | 21.31M |
| Stockholders Equity | 161.82M | 153.15M | 133.07M | 316.27M | 239.56M | 33.47M |
Cash Flow | ||||||
| Free Cash Flow | -115.09M | -130.16M | -174.14M | -147.92M | -38.23M | -6.18M |
| Operating Cash Flow | -109.06M | -122.86M | -165.41M | -131.83M | -34.08M | -5.54M |
| Investing Cash Flow | -88.84M | 68.46M | 18.71M | -47.10M | -73.63M | -1.06M |
| Financing Cash Flow | 150.95M | 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 |
|---|---|---|---|---|---|---|---|
56 Neutral | $1.30B | ― | -17.34% | ― | 83.36% | 22.27% | |
56 Neutral | $1.35B | -12.21 | -40.80% | ― | ― | ― | |
52 Neutral | $1.18B | -3.52 | -41.14% | ― | -16.50% | 33.02% | |
52 Neutral | $1.19B | ― | -64.93% | ― | -36.36% | -945.72% | |
51 Neutral | $7.86B | -0.30 | -43.30% | 2.27% | 22.53% | -2.21% | |
43 Neutral | $640.81M | ― | -112.34% | ― | 647.13% | 26.79% | |
33 Underperform | $1.08B | ― | -96.11% | ― | ― | 31.16% |
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.