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Sandoz Report the EC’s Approval of Afqlir (Biosimilar, Eylea) to Treat Neovascular Age-related Macular Degeneration (nAMD) 

Shots: 

  • The EC has approved Afqlir(2mg vial kit & pre-filled syringe for intravitreal injection), biosimilar of Bayer’s Eylea (aflibercept), with the launch anticipated in Q4’25  
  • Afqlir’s biosimilar development program included analytical, preclinical & clinical data from the Mylight trial, establishing its equivalence in terms of efficacy & safety to the reference medicine 
  • Aflibercept is a recombinant fusion protein that inhibits abnormal vessel growth by binding with VEGF-A & placental growth factor (PlGF), enhancing visual acuity & inhibiting disease progression 

Ref: Sandoz | Image: Sandoz | Press Release

Related News:- Samsung Bioepis and Biogen Report the EC’s Approval of Opuviz (Biosimilar, Eylea) 

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