Breakdown | TTM | Dec 2024 | Dec 2023 | Dec 2022 | Dec 2021 | Dec 2020 |
---|---|---|---|---|---|---|
Income Statement | ||||||
Total Revenue | 41.62M | 2.98M | 0.00 | 0.00 | 0.00 | 5.21M |
Gross Profit | 39.90M | -3.15M | -147.91M | 0.00 | 0.00 | 0.00 |
EBITDA | -200.00M | -196.34M | -193.76M | -110.75M | -160.99M | -889.00K |
Net Income | -202.01M | -195.88M | -198.13M | -121.82M | -165.37M | -3.41M |
Balance Sheet | ||||||
Total Assets | 328.16M | 297.51M | 193.85M | 360.31M | 301.86M | 54.78M |
Cash, Cash Equivalents and Short-Term Investments | 144.26M | 190.44M | 121.67M | 293.92M | 269.62M | 53.33M |
Total Debt | 121.15M | 40.79M | 13.63M | 28.75M | 10.41M | 17.52K |
Total Liabilities | 221.24M | 144.36M | 60.78M | 360.31M | 62.30M | 21.31M |
Stockholders Equity | 106.92M | 153.15M | 133.07M | -293.58M | 239.56M | 33.47M |
Cash Flow | ||||||
Free Cash Flow | -111.41M | -130.16M | -174.14M | -147.92M | -38.23M | -6.18M |
Operating Cash Flow | -104.02M | -122.86M | -165.41M | -131.83M | -34.08M | -5.54M |
Investing Cash Flow | 57.75M | 68.46M | 18.71M | -47.10M | -73.63M | -1.06M |
Financing Cash Flow | 44.55M | 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 |
---|---|---|---|---|---|---|---|
59 Neutral | £5.89B | 9.26 | -57.69% | 4.65% | 14.48% | -6.99% | |
58 Neutral | $190.87M | ― | -140.82% | ― | -48.37% | -44.70% | |
49 Neutral | $269.79M | ― | 322.49% | ― | -30.66% | 36.48% | |
46 Neutral | $177.89M | ― | -32.97% | ― | ― | ― | |
46 Neutral | $120.43M | ― | -79.02% | ― | -100.00% | 38.72% | |
43 Neutral | $317.73M | ― | -115.21% | ― | ― | 20.58% | |
38 Underperform | $264.41M | ― | -66.13% | ― | ― | 43.21% |
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.