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LAZCLUZE - Repackaging Stability

Last Updated: 08/20/2024

SUMMARY  

  • LAZCLUZE (lazertinib) is a kinase inhibitor indicated in combination with RYBREVANT (amivantamab-vmjw) 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 (Exon19del) or Exon 21 L858R substitution mutations, as detected by a United States Food and Drug Administration (FDA)-approved test.1
  • The company cannot support any practices, procedures, or storage conditions that deviate from the approved product labeling. Stability is not guaranteed for LAZCLUZE when stored outside of its original packaging. Defer to your institutional/local guidelines for guidance on repackaging pharmaceutical products.

PRODUCT LABELING

Literature Search

A literature search of MEDLINE®, Embase®, BIOSIS Previews®, and Derwent Drug File (and/or other resources, including internal/external databases) was conducted on 16 August 2024.

References

1 LAZCLUZE (lazertinib) [Prescribing Information]. Horsham, PA: Janssen Biotech, Inc.;https://www.janssenlabels.com/package-insert/product-monograph/prescribing-information/LAZCLUZE-pi.pdf.