AMD

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Contivue port delivery platform for nAMD receives CE mark
Contivue port delivery platform for nAMD receives CE mark

September 4th 2025

Roche's Contivue platform gains EU CE mark, offering innovative treatment for neovascular AMD with fewer injections and promising long-term vision outcomes.

Creation of OpZira Inc. announced following Alcon's acquisition of LumiThera
Creation of OpZira Inc. announced following Alcon's acquisition of LumiThera

September 4th 2025

Outlook Therapeutics requests Type A meeting with FDA following second CRL for ONS-5010
Outlook Therapeutics requests Type A meeting with FDA following second CRL for ONS-5010

September 3rd 2025

FDA issues complete response letter to Outlook Therapeutics for resubmitted BLA for ONS-5010
FDA issues complete response letter to Outlook Therapeutics for resubmitted BLA for ONS-5010

August 28th 2025

European Union flags outside a parliament building. Concept image for European Commission approval and European Medicines Agency regulatory decision on aflibercept biosimilar Mynzepli. Image credit: ©artjazz – stock.adobe.com
European Commission approves aflibercept biosimilar Mynzepli

August 21st 2025

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