(IN BRIEF) The European Commission has approved Ranluspec, a ranibizumab biosimilar developed by Lupin and commercialized by Sandoz, for the treatment of neovascular age-related macular degeneration and several other retinal disorders. The therapy has demonstrated comparable efficacy and safety to … Read the full press release
Posted in Business, European Union, Healthcare, Marketing, News, Pharma & Biotech, Switzerland
Tagged access to medicines, Afqlir, Basel Switzerland, biosimilars Europe, choroidal neovascularization, diabetic macular edema, diabetic retinopathy, EU commercialization rights, European Commission approval, eye disease treatment, Lucentis reference medicine, lupin, neovascular age-related macular degeneration, ophthalmology treatments, pharmaceutical partnership, ranibizumab biosimilar, Ranluspec, retinal vein occlusion, Sandoz, Sandoz and Lupin Advance European Market Entry for Ranluspec Following Regulatory Clearance, Sandoz Secures European Approval for Ranluspec to Expand Access to Biosimilar Treatment in Retinal Diseases
(IN BRIEF) Sandoz has launched Afqlir®, its biosimilar to aflibercept, across Europe following European Commission approval in 2024. Equivalent in efficacy, safety, and pharmacokinetics to Eylea®, Afqlir® provides a lower-cost treatment option for serious retinal diseases such as nAMD, RVO, … Read the full press release
Posted in Business, Healthcare, Marketing, News, Pharma & Biotech, Switzerland
Tagged aflibercept, Afqlir, anti-VEGF market, biologic medicines, biosimilar portfolio, biosimilars, Christophe Delenta, DME, European Commission approval, European Rollout of Afqlir Marks Major Step in Sandoz Expansion Across Anti-VEGF Ophthalmology Market, Eylea, intravitreal injection, mCNV, nAMD, ophthalmology, retinal diseases, RVO, Sandoz, Sustainable Healthcare, vision loss treatment
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