EligibleTrials

Lazertinib: clinical trials recruiting now

5
Recruiting trials
4
Conditions studied
34
US states with sites
21
Countries

FDA drug label

FDA-approved
Yes. Lazertinib appears in the FDA drug-label database. Marketed as LAZCLUZE.
Drug class
Kinase Inhibitor (FDA established pharmacologic class)
Mechanism of action
Kinase Inhibitors; Cytochrome P450 3A4 Inhibitors; Breast Cancer Resistance Protein Inhibitors (as stated on the FDA label)

FDA-approved use

LAZCLUZE, in combination with amivantamab, is indicated for the first-line treatment of adult patients with locally advanced or metastatic non-small cell lung cancer (NSCLC) with epidermal growth factor receptor (EGFR) exon 19 deletions or exon 21 L858R substitution mutations, as detected by an FDA-approved test [see Dosage and Administration (2.1) ] . LAZCLUZE is a kinase inhibitor indicated in combination with amivantamab for the first-line treatment of adult patients with locally advanced or metastatic non-small cell lung cancer (NSCLC) with epidermal growth factor receptor (EGFR) exon 19 deletions or exon 21 L858R substitution mutations, as detected by an FDA-approved test. ( 1 )

FDA label via openFDA

Phase breakdown

Phase 2 5

Conditions being studied

ConditionTrials
Lung cancer · Lazertinib for Lung cancer5
Carcinoma, Non-Small-Cell Lung · Lazertinib for Carcinoma, Non-Small-Cell Lung3
Lazertinib1
Non-Small Cell Lung Cancer Metastatic1

Recruiting trials involving Lazertinib

Common questions

Is Lazertinib FDA-approved?

Yes, marketed as LAZCLUZE.

How many recruiting trials involve Lazertinib?

5 recruiting trials across 4 conditions.

Is this list of trials complete?

No. For the full record, search ClinicalTrials.gov.

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