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UK Medicines and Healthcare Products Regulatory Agency (MHRA) Issues an Early Access to Medicines Scheme (EAMS) Positive Scientific Opinion for Tepotinib for the Treatment of Advanced NSCLC with METex14 Skipping Alterations


Feltham (Merck)
– Merck announced today that the UK Medicines and Healthcare Products Regulatory Agency (MHRA) has issued an Early Access to Medicines Scheme (EAMS) positive scientific opinion for tepotinib for the treatment of adult patients with advanced Non-Small Cell Lung Cancer (NSCLC) harbouring mesenchymal-epithelial transition factor gene (MET) exon 14 (METex14) skipping alterations.1 With this approval, the MHRA have confirmed a positive benefit-risk ratio of tepotinib in this patient population.
The positive scientific opinion is based on results from the Phase II VISION study evaluating tepotinib as monotherapy in patients with advanced or metastatic NSCLC with METex14 skipping alterations, prospectively assessed by liquid biopsy or tissue biopsy. The VISION study demonstrated an objective response rate by independent review of 46% (95% confidence interval [CI], 36 to 57) in the combined-biopsy group. Data from the primary analysis of the VISION study were published in The New England Journal of Medicine (NEJM) on 29 May 2020.

Lung cancer is the third most common cancer in the UK, accounting for 13% of all new cancer cases in 2017, and was the leading cause of cancer related death in the UK in 2018. NSCLC is the most common type of lung cancer and accounts for approximately 80-85% of all lung cancer diagnoses.4 METex14 alterations occur in approximately 3-4% of NSCLC cases and generally exhibit a poorer clinical prognosis compared with other types of NSCLC. 

Dr Mike England, Medical Director, Merck UK & Ireland said: “We are delighted by the MHRA’s positive decision to provide early access to tepotinib for patients with advanced NSCLC harbouring METex14 skipping alterations in the United Kingdom, as there is a significant unmet need for new treatment options for these patients, who typically have a poor clinical prognosis. We believe this is a major advance in the treatment of these patients.
Tepotinib is not licensed in the United Kingdom for the treatment of advanced NSCLC with METex14 skipping alterations.  
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