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NCE-1 Intelligence & Market Opportunity

Tepmetko

Tepotinib
Anticancer
Oral Tablet

Tepmetko (tepotinib) targets MET exon 14 skipping alterations, which drive a small but distinct subset of lung cancer that had few targeted options until recently.

Taken once daily, tepotinib selectively blocks MET kinase signaling to slow tumor growth in adults with metastatic non-small cell lung cancer harboring MET exon 14 skipping alterations. It was the first once-daily oral MET inhibitor cleared by the FDA, differentiating it from twice-daily alternatives.

Tepmetko’s accelerated approval was later converted to full approval on confirmatory data, removing its main regulatory overhang, and it faces no generic competition. It is a core comparator in MET-altered NSCLC and relevant to biomarker-driven trial planning in lung cancer.

Approval Date
02-Mar-21
NCE-1 Date
02-Mar-25
NCE Date
02-Mar-26
Commercial snapshot

Market performance & projections

Revenue ($M)
NA
CAGR (%)
NA
Projected sales, 2026–2032 ($M)
Analyst projection, $M per year
2026
137
2027
142
2028
149
2029
157
2030
165
2031
105
2032
89
Molecule profile

Details & specifications

Molecule
Tepotinib
Innovator
EMD SERONO, INC.
Dosage Form
Oral Tablet
Strength
EQ 225 mg base
Therapeutic Category
Anticancer
Usage
To treat non-small cell lung cancer
Good to know

Frequently asked questions

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