Oops, you're using an old version of your browser so some of the features on this page may not be displaying properly.

MINIMAL Requirements: Google Chrome 24+Mozilla Firefox 20+Internet Explorer 11Opera 15–18Apple Safari 7SeaMonkey 2.15-2.23

EMA Recommends Granting a Marketing Authorisation for Capmatinib

It is intended for treatment of patients with advanced NSCLC harbouring alterations leading to METex14 skipping
13 May 2022
Anticancer agents & Biologic therapy;  Lung and other thoracic tumours;  Personalised medicine

On 22 April 2022, the European Medicines Agency’s (EMA’s) Committee for Medicinal Products for Human Use adopted a positive opinion, recommending the granting of a marketing authorisation for the medicinal product capmatinib (Tabrecta), intended for treatment of patients with advanced non-small cell lung cancer (NSCLC) harbouring alterations leading to mesenchymal-epithelial transition factor gene exon 14 (METex14) skipping.

The applicant for this medicinal product is Novartis Europharm Limited.

Tabrecta will be available as 150 mg and 200 mg film-coated tablets. The active substance of Tabrecta is capmatinib, a MET inhibitor (ATC code: L01EX17) which blocks MET phosphorylation and MET-dependent downstream signalling.

The benefits of Tabrecta are its objective response rate and response duration in patients with NSCLC harbouring alterations leading to METex14 skipping.

The most common side effects are peripheral oedema, nausea, fatigue, vomiting, dyspnoea and decreased appetite.

The full indication is:

Tabrecta as monotherapy is indicated for the treatment of adult patients with advanced NSCLC harbouring alterations leading to METex14 skipping, who require systemic therapy following prior treatment with immunotherapy and/or platinum-based chemotherapy.

Tabrecta should be prescribed by physicians experienced in the use of anticancer medicinal products.

Detailed recommendations for the use of this product will be described in the summary of product characteristics, which will be published in the European public assessment report and made available in all official European Union languages after the marketing authorisation has been granted by the European Commission.

Summaries of positive opinion are published without prejudice to the Commission decision, which will normally be issued 67 days from adoption of the opinion.

This site uses cookies. Some of these cookies are essential, while others help us improve your experience by providing insights into how the site is being used.

For more detailed information on the cookies we use, please check our Privacy Policy.

Customise settings
  • Necessary cookies enable core functionality. The website cannot function properly without these cookies, and you can only disable them by changing your browser preferences.