Regulatory approval

Published by the European Medicines Agency. Approved

Rozlytrek as monotherapy is indicated for the treatment of adult patients with ROS1-positive, advanced non-small cell lung cancer (NSCLC) not previously treated with ROS1 inhibitors.

This is written in the approval document.

Citation

Roche Registration GmbH. Rozlytrek (entrectinib) [product information]. European Medicines Agency website. https://www.ema.europa.eu/en/documents/product-information/rozlytrek-epar-product-information_en.pdf. Revised July 2023. Accessed March 22, 2024.

Therapeutic response

Precision oncology relationships for therapeutic response derived from this regulatory approval.

Organizations
Biomarkers
Cancer types
Therapies
Organizations Biomarkers Cancer types Therapies
EMA (1) v::ROS1 Non-Small Cell Lung Cancer Entrectinib

Contributions

Date Contributor Description
2024-10-20 Van Allen lab Adding EMA approvals for use to database
2020-07-31 European Medicines Agency Indication received approval from the European Commission.