Lazcluze

lazertinib · Janssen Cilag International NV
AUTHORISED IN THE EU

What Lazcluze is used for

Lazcluze in combination with amivantamab is indicated for the first line treatment of adult patients with advanced non small cell lung cancer (NSCLC) with EGFR exon 19 deletions or exon 21 L858R substitution mutations.

Approved use, as published by the European Medicines Agency.

Key facts

Brand
Lazcluze
Active substance
lazertinib
Disease area
Carcinoma, Non-Small-Cell Lung
Medicine group
Antineoplastic agents
ATC code
L01EB09
Marketing authorisation holder
Janssen Cilag International NV
Authorised in the EU since
2025

Official information

Specialist medicine: started and supervised by a specialist doctor or hospital. This page is a plain-language summary of public official information, not medical advice; follow your doctor and the official product information.

Common questions

What is Lazcluze used for?

Lazcluze in combination with amivantamab is indicated for the first line treatment of adult patients with advanced non small cell lung cancer (NSCLC) with EGFR exon 19 deletions or exon 21 L858R substitution mutations.

What is the active substance in Lazcluze?

Lazcluze contains lazertinib.

Who makes Lazcluze?

The EU marketing authorisation holder is Janssen Cilag International NV.

Source: European Medicines Agency medicines data (ema.europa.eu), reproduced with acknowledgement of the source. Page made 5 November 2026 by Satya Babu.

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