EMA European Union — centrally authorised medicines
Enrylaze Jazz Pharmaceuticals Ireland Limited · Authorised · authorised 15 Sep 2023 · ATC L01XX02
Therapeutic indication (EMA)
Enrylaze is indicated as a component of a multi-agent chemotherapeutic regimen for the treatment of acute lymphoblastic leukaemia (ALL) and lymphoblastic lymphoma (LBL) in adult and paediatric patients (1 month and older) who developed hypersensitivity or silent inactivation to E. coli-derived asparaginase.
Canada Canada — marketed products (Health Canada)
| Brand | DIN | Strength | Form · route | Company |
| RYLAZE | 02530406 | 10 MG / 0.5 ML | SOLUTION · INTRAMUSCULAR | JAZZ PHARMACEUTICALS IRELAND LIMITED |
Values as published by each source: SFDA human drug list (4-2026, as published by the Council of Health Insurance; indications from the CHI Daman Drug Formulary), Drugs@FDA, EMA medicines data, Health Canada Drug Product Database (Open Government Licence – Canada), CMS NADAC, NHS Drug Tariff Part VIIIA (NHSBSA Copyright, Open Government Licence v3.0), WHO Model List of Essential Medicines (CC BY 3.0 IGO; regrouped by active substance, not created by WHO), EMA PRAC, US FDA safety-related labeling changes and MHRA Drug Safety Update (Open Government Licence v3.0). Sources and reuse. Not a substitute for the official registers or the product information.