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Merus (MRUS) investor relations material
Merus Corporate Presentation summary
Complete event summary combining all related documents: earnings call transcript, report, and slide presentation.Clinical pipeline and product highlights
Petosemtamab shows strong efficacy in 1L and 2L+ r/m HNSCC and mCRC, with phase 3 trials enrolling and robust interim data in both indications.
Bizengri® (zenocutuzumab) received accelerated FDA approval for NRG1+ pancreatic adenocarcinoma and NSCLC.
MCLA-129 demonstrates clinical activity in EGFRm and METex14 NSCLC, with ongoing trials in combination with chemotherapy.
Multiple collaboration programs from Multiclonics® platforms are advancing into the clinic.
Proprietary Biclonics® and Triclonics® platforms enable development of bispecific and trispecific antibodies and ADCs.
Petosemtamab clinical data and safety
In 1L mCRC, petosemtamab + FOLFOX/FOLFIRI showed an 80% response rate; in 2L, 62%; and in 3L+ monotherapy, 10%.
In 1L PD-L1+ r/m HNSCC with pembrolizumab, confirmed ORR was 63%, median PFS 9 months, and 12-month OS rate 79%.
In 2L+ r/m HNSCC monotherapy, ORR was 36%, with median DOR 6.2 months and OS 11.4 months.
Safety profile is favorable, with no new safety signals and manageable side effects across studies.
Phase 3 trials in r/m HNSCC expected to be substantially enrolled by year end 2025, with topline readouts in 2026.
Market opportunity and financials
Estimated 2024 worldwide sales: r/m HNSCC $4B, mCRC $7.2B, with significant unmet need and high prevalence.
Petosemtamab positioned as potential first and best-in-class bispecific in r/m HNSCC and mCRC.
Cash and cash equivalents of $817M, expected to fund operations through multiple milestones into at least 2028.
Patent estate for petosemtamab extends to at least 2045, covering composition, methods, and combinations.
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