Food and Drug Administration approved ibrutinib (Imbruvica, Pharmacyclics LLC) for pediatric patients

On August 24, 2022, the Food and Drug Administration approved ibrutinib (Imbruvica, Pharmacyclics LLC) for pediatric patients ≥ 1 year of age with chronic graft versus host disease (cGVHD) after failure of 1 or more lines of systemic therapy. Formulations include capsules, tablets, and oral suspension.

For more information, read the FDA Announcement or Press Release.