Breakdown | ||||
Dec 2024 | Dec 2023 | Dec 2022 | Dec 2021 | Dec 2020 |
---|---|---|---|---|
Income Statement | Total Revenue | |||
40.50M | 36.85M | 26.58M | 43.00K | 828.00K | Gross Profit |
40.50M | -111.41M | 25.65M | -131.97M | -66.21M | EBIT |
-73.34M | -170.96M | -204.69M | -169.71M | -87.69M | EBITDA |
-63.27M | -166.08M | -199.96M | -167.94M | -86.68M | Net Income Common Stockholders |
-69.19M | -171.67M | -207.54M | -169.21M | -88.40M |
Balance Sheet | Cash, Cash Equivalents and Short-Term Investments | |||
134.62M | 209.08M | 280.71M | 177.95M | 255.09M | Total Assets |
144.66M | 226.06M | 334.34M | 206.11M | 273.40M | Total Debt |
17.65M | 33.83M | 36.30M | 38.18M | 16.57M | Net Debt |
-90.10M | -140.73M | -244.41M | -139.77M | -238.52M | Total Liabilities |
154.17M | 189.16M | 242.28M | 84.37M | 45.31M | Stockholders Equity |
-9.51M | 36.90M | 92.06M | 121.74M | 228.09M |
Cash Flow | Free Cash Flow | |||
-82.47M | -171.05M | -51.56M | -140.64M | -75.17M | Operating Cash Flow |
-82.34M | -168.88M | -49.36M | -139.99M | -74.70M | Investing Cash Flow |
11.44M | 119.88M | -152.72M | -648.00K | 37.03M | Financing Cash Flow |
4.09M | 94.67M | 153.02M | 63.65M | 230.41M |
Name | Overall Rating | Market Cap | P/E Ratio | ROE | Dividend Yield | Revenue Growth | EPS Growth |
---|---|---|---|---|---|---|---|
67 Neutral | $6.83B | 29.54 | 19.71% | ― | 52.97% | ― | |
58 Neutral | $6.26B | 285.53 | 12.21% | ― | 40.80% | 100.62% | |
52 Neutral | $5.67B | ― | -31.26% | ― | 104.04% | 87.80% | |
49 Neutral | $6.85B | 0.81 | -52.91% | 2.50% | 17.48% | 1.17% | |
46 Neutral | $79.49M | ― | -49.85% | ― | 155.26% | -640.36% | |
40 Underperform | $35.01M | ― | 41.08% | ― | -0.55% | 49.85% | |
36 Underperform | $47.30M | ― | -505.14% | ― | 9.88% | 62.31% |
On March 3, 2025, Mersana Therapeutics announced positive initial Phase 1 clinical data for its lead ADC candidate, Emi-Le, and received a second Fast Track designation from the FDA. The company also initiated an expansion cohort for patients with triple-negative breast cancer and plans to present further clinical data in 2025. Financial results for 2024 showed a net loss reduction compared to 2023, with increased collaboration revenue and decreased R&D and G&A expenses due to restructuring and discontinued projects.
On February 5, 2025, Mersana Therapeutics updated its corporate presentation on its website for investors to access. The information shared is not considered filed under the Securities Exchange Act of 1934 and is not subject to associated liabilities, nor is it incorporated by reference in any SEC filings unless specifically stated.
Mersana Therapeutics announced positive initial results from their Phase 1 clinical trial of emiltatug ledadotin (Emi-Le), showing promising efficacy and a favorable safety profile, particularly in heavily pre-treated triple-negative breast cancer (TNBC) patients. The U.S. FDA granted an additional Fast Track designation for Emi-Le, enhancing its potential market impact as Mersana continues dose expansion trials and explores further clinical benefits, which could strengthen their position in the ADC landscape.