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 |
---|---|---|---|---|---|---|---|
50 Neutral | $2.33B | ― | -43.94% | ― | -83.18% | -144.95% | |
49 Neutral | $6.95B | 0.67 | -53.43% | 2.47% | 22.78% | 1.44% | |
46 Neutral | $3.54B | ― | -19.20% | ― | -89.95% | -123.71% | |
45 Neutral | $255.76M | ― | -136.88% | ― | ― | 20.58% | |
39 Underperform | $108.70M | ― | -98.10% | ― | -58.64% | -40.05% | |
39 Underperform | $931.66M | ― | -54.00% | ― | 59.55% | 3.09% | |
39 Underperform | $492.82M | ― | -36.36% | ― | 174.98% | 25.06% |
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.
Prime Medicine, Inc. has updated its corporate presentation to reflect significant advancements in its gene editing programs. The company has initiated a Phase 1/2 trial for PM359 in CGD and is progressing with Wilson’s Disease and CF programs, leveraging strategic collaborations to expand their pipeline. The company aims to achieve clinical validation and sustainable value creation, supported by new partnerships and a strong financial position.