Merck announced on Thursday that the European Commission has granted marketing authorization for Keytruda, its blockbuster immunotherapy, in the treatment of operable non-small cell lung cancer at high risk of recurrence.

Brussels' approval covers, more specifically, the combination of Keytruda with chemotherapy in the neoadjuvant (pre-operative) treatment of the disease, then as monotherapy as adjuvant therapy.

Merck points out that this is the first time that an anti-PD-1/L1 therapy has been approved for the treatment of operable non-small cell lung cancer in Europe.

This is the sixth indication for Keytruda in the treatment of bronchial cancer on the Old Continent.

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