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European Commission Approves Rylaze for ALL and Lymphoblastic Lymphoma

The European Commission has granted marketing authorization for Rylaze for use as a component of a multi-agent chemotherapeutic regimen for the treatment of patients with acute lymphoblastic leukemia and lymphoblastic lymphoma in adult and pediatric patients 1 month and older who developed hypersensitivity or silent inactivation to E. coli–derived asparaginase.
Carmelo Rizzari Robert Iannone University Of Milano Jazz Pharmaceuticals European Union European Commission

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Lonza Confirms Details of Capital Markets Day and Reconfirms Outlook 2023

Lonza Group AG / Key word(s): Forecast Lonza Confirms Details of Capital Markets Day and Reconfirms Outlook 2023 21-Sep-2023 / 07:00 CET/CEST Release of an ad hoc announcement pursuant to Art. 53 LR The issuer is solely responsible for the content of this announcement. Ad hoc announcement pursua...
Lonza Visp Lyle Wheeler Albertm Baehny Swiss Exchange Lonza Group Lonza Group Ltd

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