Prognia
Drug Database
🇪🇺EU · EMAAuthorisedATC: L01ED03

Alecensa(alectinib hydrochloride)

Carcinoma, Non-Small-Cell Lung

Marketing Authorisation Holder: Roche Registration GmbH

EMA Authorisation: 16/02/2017

INN: alectinib

Indication

Adjuvant treatment of resected non small cell lung cancer (NSCLC) Alecensa as monotherapy is indicated as adjuvant treatment following complete tumour resection for adult patients with ALK positive NSCLC at high risk of recurrence (see section 5.1 for selection criteria).Treatment of advanced NSCLCAlecensa as monotherapy is indicated for the first line treatment of adult patients with ALK positive advanced NSCLC.Alecensa as monotherapy is indicated for the treatment of adult patients with ALK positive advanced NSCLC previously treated with crizotinib.

Official EMA Resources

View on EMA (ema.europa.eu)

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Medical disclaimer: This information is intended for qualified healthcare professionals. Always verify with the official EMA Summary of Product Characteristics (SmPC) before clinical use.