Merck KGaA of Darmstadt, which trades as EMD Serono in North America, sells the anti-PD-L1 antibody avelumab, cetuximab outside the United States and the MET inhibitor tepotinib, and bought SpringWorks Therapeutics in 2025 to add nirogacestat and mirdametinib for rare tumours.
Merck KGaA, the Darmstadt science and technology company that is distinct from the US Merck & Co., runs its healthcare business as EMD Serono in the United States and Canada. Its oncology medicines include avelumab (Bavencio), an anti-PD-L1 antibody used as maintenance in urothelial cancer and in Merkel cell carcinoma; cetuximab (Erbitux), which it markets outside North America; and tepotinib (Tepmetko) for MET exon 14-skipping non-small-cell lung cancer. On 1 July 2025 it completed its acquisition of SpringWorks Therapeutics at USD 47 a share in cash, bringing the gamma-secretase inhibitor nirogacestat for desmoid tumours and the MEK inhibitor mirdametinib for neurofibromatosis-related plexiform neurofibromas. In April 2025 it exercised its global option on Abbisko's CSF-1R inhibitor pimicotinib, which China's regulator approved in December 2025 for tenosynovial giant cell tumour. Company facts are from FDA approval records, SpringWorks' closing filing with the SEC and Abbisko's Hong Kong exchange announcements.
Avelumab is a PD-L1 blocker given as maintenance after chemotherapy for advanced bladder cancer, which lengthened survival by about seven months.
Cetuximab is a chimeric antibody that blocks the EGFR growth receptor. It is used with FOLFIRI or FOLFOX in RAS wild-type, left-sided bowel cancer, with encorafenib in BRAF V600E disease, with KRAS G12C inhibitors, and with radiation or chemotherapy in head and neck cancer; RAS-mutant tumours gain nothing and may be harmed, so RAS testing comes first.
Capmatinib and tepotinib are two pills for the roughly 3% of lung cancers with a MET exon 14 skipping mutation.
Nirogacestat is the first approved medicine for desmoid tumours, locally invasive growths that do not spread but can be crippling; it works by blocking Notch signalling.
Mirdametinib (Gomekli in the US, Ezmekly in Europe) is a MEK-blocking capsule or dispersible tablet for adults and children with neurofibromatosis type 1 whose plexiform neurofibromas cannot be removed surgically; it is the first such drug approved for adults.
Precemtabart tocentecan is an experimental antibody-drug conjugate from EMD Serono Research & Development Institute in phase 3 trials for colorectal cancer, aimed at CEACAM5.
Pimicotinib is an oral kinase inhibitor from Merck Healthcare KGaA, Darmstadt, Germany, an affiliate of Merck KGaA, Darmstadt, Germany, in registered phase 2 trials for tenosynovial giant cell tumour.
Tepotinib is a once-daily targeted pill for lung cancers driven by a MET exon 14 skipping mutation, and the MET inhibitor NICE funds in England.
Xevinapant was a tablet meant to make head and neck cancer cells easier to kill with chemoradiation by removing the proteins that stop them dying. A promising mid-stage trial was followed by a phase 3 that was stopped in 2024 because it was not working.
Shares Head and neck squamous cell carcinoma and the tag fda-oce-applicant.
Shares Non-small-cell lung cancer and the tag fda-oce-applicant.
Shares SpringWorks Therapeutics (Merck KGaA), Nirogacestat, Desmoid tumour.
Shares VISION (tepotinib), Tepotinib, MET exon 14 and MET-amplified non-small-cell lung cancer.
Shares Xevinapant, EXTREME, JAVELIN Head and Neck 100, Cetuximab.
Shares Single-use bioprocessing systems, Downstream purification (Protein A capture, viral clearance, polishing), The ADC supply chain (antibody, payload-linker, conjugation, fill).
Shares Avelumab, Merkel cell carcinoma, Head and neck squamous cell carcinoma, Non-small-cell lung cancer.
Shares JAVELIN Bladder 100, Avelumab.
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