Eylea HD (aflibercept) developers Regeneron Pharmaceuticals (Nasdaq: REGN) and Bayer (BAYN: DE) have announced positive Phase III results, from the QUASAR study.
The trial tests the therapy in macular edema following retinal vein occlusion (RVO). There were non-inferior vision gains for the product, which offers extended dosing intervals compared to regular Eylea.
The companies plan to submit a supplementary application to the US Food and Drug Administration in the first quarter of 2025, as well as in other countries.
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