Prognia
Drug Database
🇪🇺EU · EMAAuthorisedATC: L01EB

Aumseqa(Aumolertinib mesilate)

Carcinoma, Non-Small-Cell Lung

Marketing Authorisation Holder: SFL Pharmaceuticals Deutschland GmbH

EMA Authorisation: 12/02/2026

INN: Aumolertinib

Indication

Aumseqa as monotherapy is indicated for:- the first-line treatment of adult patients with advanced non-small cell lung cancer (NSCLC)whose tumours have EGFR exon 19 deletions or exon 21 (L858R) substitution mutations (forbiomarker-based patient selection, see section 4.2).- the treatment of adult patients with advanced EGFR T790M mutation-positive NSCLC (forbiomarker-based patient selection, see section 4.2)

Official EMA Resources

View on EMA (ema.europa.eu)

AI Drug & Interaction Analysis

Free account required

Ask Prognia AI about Aumseqa — dosing recommendations, drug interactions, and current guideline evidence from ESC, EMA, NICE and more.

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