| Breakdown | TTM | Dec 2024 | Dec 2023 | Dec 2022 | Dec 2021 | Dec 2020 |
|---|---|---|---|---|---|---|
Income Statement | ||||||
| Total Revenue | 51.17M | 34.88M | 39.81M | 38.84M | 43.15M | 24.51M |
| Gross Profit | -111.30M | 12.96M | 29.31M | 28.88M | -43.12M | -32.82M |
| EBITDA | -323.66M | -260.24M | -139.50M | -148.26M | -77.75M | -60.93M |
| Net Income | -334.90M | -207.85M | -140.34M | -122.52M | -58.70M | -70.00M |
Balance Sheet | ||||||
| Total Assets | 771.99M | 785.13M | 455.49M | 376.54M | 456.60M | 231.22M |
| Cash, Cash Equivalents and Short-Term Investments | 542.95M | 537.03M | 355.18M | 290.23M | 410.43M | 207.75M |
| Total Debt | 10.52M | 9.91M | 12.16M | 13.47M | 3.75M | 3.95M |
| Total Liabilities | 110.36M | 134.77M | 99.15M | 129.49M | 140.40M | 128.95M |
| Stockholders Equity | 661.63M | 647.93M | 356.34M | 247.06M | 316.20M | 102.26M |
Cash Flow | ||||||
| Free Cash Flow | -317.87M | -187.50M | -146.19M | -157.54M | -60.50M | -81.19M |
| Operating Cash Flow | -317.27M | -185.84M | -142.21M | -149.90M | -59.63M | -79.90M |
| Investing Cash Flow | -93.55M | -220.22M | -27.02M | 2.80M | -146.62M | -1.49M |
| Financing Cash Flow | 354.22M | 494.01M | 230.09M | 58.74M | 281.95M | 39.52M |
Name | Overall Rating | Market Cap | P/E Ratio | ROE | Dividend Yield | Revenue Growth | EPS Growth |
|---|---|---|---|---|---|---|---|
80 Outperform | $6.15B | 31.80 | 19.66% | ― | 54.51% | 275.94% | |
74 Outperform | $6.30B | 9.17 | ― | ― | 97.54% | ― | |
60 Neutral | $4.47B | ― | -34.53% | ― | ― | -0.06% | |
56 Neutral | $10.63B | ― | -32.44% | ― | 106.27% | -43.90% | |
52 Neutral | $7.28B | ― | -51.57% | ― | 57.54% | -36.57% | |
51 Neutral | $7.86B | -0.30 | -43.30% | 2.27% | 22.53% | -2.21% | |
45 Neutral | $2.28B | ― | -28.96% | ― | 23.73% | 30.16% |
Merus NV faces significant business risks due to its reliance on the unproven ADClonics technology platform for producing antibody drug conjugates. The company has yet to secure regulatory approval for its innovative approach, which involves attaching a linker and payload to a proprietary antibody format. This dependency on third-party suppliers for critical components such as linkers and payloads introduces vulnerabilities, as these materials have occasionally failed to meet expectations, potentially leading to disruptions. Furthermore, quality issues, contamination, and the presence of active pathogens in these materials could severely impact Merus NV’s ability to develop and commercialize its ADClonics candidates, posing a threat to its financial stability and operational success.
Merus NV faces significant business risks due to potential delays or failure in completing its transaction with Genmab A/S. The uncertainty surrounding the completion of the Transactions could adversely impact Merus NV’s share price, financial condition, and operational prospects. Additionally, the company may incur substantial costs, face negative publicity, and experience difficulties in maintaining key relationships and attracting talent. The market’s perception of the likelihood of the Transactions’ success could further lead to fluctuations in the company’s share price.
Merus N.V. recently updated its Phase 2 clinical study evaluating zenocutuzumab (MCLA-128) in patients with specific cancer types. Officially titled ‘A Phase 2 Study Evaluating Activity of Zenocutuzumab (MCLA-128) in Patients With or Without Molecularly Defined Cancers,’ the study aims to assess the efficacy of zenocutuzumab in treating NSCLC with NRG1 fusion and metastatic castration-resistant prostate cancer (mCRPC). This study is significant as it explores targeted treatments for these challenging cancer types.
On September 29, 2025, Merus N.V. entered into a Transaction Agreement with Genmab A/S and its subsidiary, Genmab Holding II B.V., for a tender offer to purchase all outstanding shares of Merus at $97.00 per share. This agreement, which includes subsequent offering periods and back-end transactions, aims to make Merus an indirect wholly owned subsidiary of Genmab. The transaction will lead to the delisting of Merus’s shares from Nasdaq and cessation of its reporting obligations. The agreement is subject to various conditions, including shareholder approval and regulatory clearances, and outlines specific termination rights and fees.
The most recent analyst rating on (MRUS) stock is a Hold with a $97.00 price target. To see the full list of analyst forecasts on Merus stock, see the MRUS Stock Forecast page.
Merus N.V. is conducting a Phase 3 study titled ‘A Phase 3 Open-label, Randomized Controlled Study to Evaluate the Efficacy and Safety of Petosemtamab Compared With Investigator’s Choice Monotherapy Treatment in Previously Treated Patients With Incurable, Metastatic/Recurrent Head and Neck Squamous Cell Carcinoma.’ The study aims to assess the effectiveness and safety of petosemtamab against standard monotherapy options in patients with advanced head and neck squamous cell carcinoma (HNSCC), a significant area of unmet medical need.
Merus N.V. is conducting a Phase 3 clinical study titled ‘A Phase 3 Study to Evaluate Petosemtamab Plus Pembrolizumab vs Pembrolizumab in First-line Treatment of Head and Neck Cancer (LiGeR – HN1).’ The study aims to assess the efficacy and safety of combining petosemtamab with pembrolizumab compared to pembrolizumab alone in treating recurrent or metastatic PD-L1+ head and neck squamous cell carcinoma. This research is significant as it explores potential advancements in cancer treatment, offering hope for improved patient outcomes.
Merus N.V., a Netherlands-based oncology company, focuses on developing innovative antibody therapeutics, with a notable presence in the biopharmaceutical industry. The company is known for its proprietary Triclonics® platform used in the development of multispecific antibody products.