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GSK To Address Multiple Myeloma With First-In-Class Blenrep In EU

Approval Conditional On Further Studies, Risk Management Plan

 
• By John Davis

The European Commission’s approval of GlaxoSmithKline’s Blenrep is one of the first major fruits of a refocused pipeline and development strategy at the big pharma company.  

Approved_Signature
• Source: Shutterstock

GlaxoSmithKline plc has taken another important step back into the anticancer sector with the European Commission’s conditional approval of the company’s late-stage multiple myeloma therapy, Blenrep (belantamab mafodotin), announced on the 26 August. 

The product is an antibody drug conjugate comprising a humanized anti-B cell maturation antigen (BCMA) monoclonal antibody conjugated to cytotoxic...

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