Merus' Petosemtamab Shows Promise in HNSCC and NSCLC Trials, Bolstering Investment Potential
- Merus' petosemtamab demonstrates a 42.5% overall response rate in Phase 2 trials for second-line or higher head and neck squamous cell carcinoma (HNSCC).
- In combination with pembrolizumab, petosemtamab shows a 60% objective response rate for first-line HNSCC treatment, aligning with optimistic analyst projections.
- MCLA-129 demonstrates efficacy in MET exon 14 EGFR NSCLC patients, achieving a 43.5% overall response rate, suggesting potential in specific genetic mutations.
- Analysts project revenue growth for Merus, with estimates of $112 million for 2025, driven by clinical trial successes and potential regulatory approvals.
Merus N.V. (NASDAQ: MRUS) is gaining attention in the oncology space as its innovative bispecific antibody therapies advance through clinical trials. The company's lead candidate, petosemtamab, is showing promising results in treating head and neck squamous cell carcinoma (HNSCC), while other pipeline assets are also demonstrating potential in non-small cell lung cancer (NSCLC).
Petosemtamab (peto) has emerged as a frontrunner in Merus's clinical pipeline, particularly for HNSCC treatment. Data from a Phase 2 trial in second-line or higher (2L+) HNSCC patients revealed an overall response rate (ORR) of 42.5%, a median progression-free survival (mPFS) of 5.1 months, and an overall survival (OS) of 12.5 months. These findings, presented at the ESMO Asia conference, build upon previous data and are expected to surpass cetuximab 2L+ benchmarks. A dose optimization cohort indicated that a 1500mg dose of peto had improved efficacy compared to a 1100mg dose, potentially enhancing its therapeutic profile. The positive outcomes from these trials have increased confidence in the potential success of the upcoming Phase 3 LiGeR-HN2 trial.
In combination with pembrolizumab for first-line HNSCC treatment, peto showed an impressive 60% objective response rate, aligning with analysts' upside case scenarios. This data is expected to mature further, with additional results anticipated in the near future.
MCLA-129, another promising candidate in Merus's pipeline, has demonstrated efficacy in MET exon 14 EGFR NSCLC patients, achieving a 43.5% ORR. This data suggests potential in addressing specific genetic mutations in non-small cell lung cancer.
Analysts project revenues of $44 million for 2023, $42 million for 2024, and a significant jump to $112 million for 2025. It's important to note that these projections are subject to change based on clinical trial outcomes and potential regulatory approvals.
The immuno-oncology market remains highly competitive, with several large pharmaceutical companies and biotechs vying for market share. Merus's innovative antibody platform sets it apart, but the company will need to navigate carefully through clinical development and potential commercialization to establish a strong market position.
Analyst Charles Zhu from LifeSci Capital maintained a Buy rating on Merus (MRUS) and keeping the price target at $100.00. Zhu's rating is based on several promising aspects of Merus’s current and future prospects. The company has been making significant strides with its clinical trials, particularly with its EGFR x Lgr5 bispecific petosemtamab, which shows potential in treating HNSCC and CRC. The management team’s strong execution and the promising clinical efficacy of petosemtamab in both HPV+ and HPV- HNSCC settings have been highlighted as key factors.
Furthermore, Merus’s recent achievements, such as the regulatory approval of Zenocutuzumab in NRG1+ NSCLC and PDAC, along with securing a commercial partnership, are vital milestones that bolster its growth outlook. With a robust pipeline and strategic collaborations, Merus is poised to achieve additional key milestones in 2025, making it an attractive investment opportunity.

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Charles Zhu of LifeSci Capital maintains a Buy rating on Merus (MRUS) with a $100 target, citing promising clinical tria...
[2]
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