Breakdown | TTM | Dec 2024 | Dec 2023 | Dec 2022 | Dec 2021 | Dec 2020 |
---|---|---|---|---|---|---|
Income Statement | ||||||
Total Revenue | 4.96M | 2.98M | 0.00 | 0.00 | 0.00 | 5.21M |
Gross Profit | 3.10M | 2.98M | -4.65M | -12.01M | -4.86M | 2.23M |
EBITDA | -199.25M | -196.34M | -193.76M | -110.75M | -160.99M | -889.00K |
Net Income | -199.28M | -195.88M | -198.13M | -121.82M | -165.37M | -3.41M |
Balance Sheet | ||||||
Total Assets | 279.01M | 297.51M | 193.85M | 360.31M | 301.86M | 54.78M |
Cash, Cash Equivalents and Short-Term Investments | 98.34M | 190.44M | 121.67M | 293.92M | 269.62M | 53.33M |
Total Debt | 119.74M | 40.79M | 13.63M | 28.75M | 10.41M | 17.52M |
Total Liabilities | 218.15M | 144.36M | 60.78M | 44.04M | 62.30M | 21.31M |
Stockholders Equity | 60.86M | 153.15M | 133.07M | 316.27M | 239.56M | 33.47M |
Cash Flow | ||||||
Free Cash Flow | -107.00M | -130.16M | -174.14M | -147.92M | -38.23M | -6.18M |
Operating Cash Flow | -99.94M | -122.86M | -165.41M | -131.83M | -34.08M | -5.54M |
Investing Cash Flow | 53.62M | 68.46M | 18.71M | -47.10M | -73.63M | -1.06M |
Financing Cash Flow | 44.71M | 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 |
---|---|---|---|---|---|---|---|
52 Neutral | $391.83M | -2.26 | -31.51% | ― | ― | ― | |
51 Neutral | $291.34M | -1.14 | -176.57% | ― | -41.97% | -20.86% | |
46 Neutral | $115.50M | -1.42 | ― | ― | -100.00% | 62.82% | |
43 Neutral | $912.36M | ― | -154.81% | ― | 739.42% | 24.90% | |
40 Neutral | $274.74M | -3.92 | 98.35% | ― | -31.30% | 36.26% | |
38 Underperform | $370.32M | -2.62 | ― | ― | ― | -5.57% | |
51 Neutral | $7.86B | -0.30 | -43.30% | 2.27% | 22.53% | -2.21% |
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.