Xbrane And Stada Celebrate Major Milestone With EU Filing For Lucentis Rival

Xlucane Asset Joins Bioeq/Formycon FYB201 Biosimilar With EMA

Xbrane Biopharma has taken a key step on its journey to begin generating cash from operations by early 2024 at the latest, after its Xlucane biosimilar ranibizumab asset was submitted to the European Medicines Agency by co-development and commercialization partner Stada.

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Xbrane reported top-line Phase III data in June • Source: Shutterstock

The potential for further biosimilar competition to Lucentis (ranibizumab) in Europe continues to build, with Stada becoming the latest company to submit a marketing authorization application for a biosimilar product, partner Xbrane Biopharma’s proposed Xlucane biosimilar candidate, to the European Medicines Agency.

The Swedish player has disclosed that the MAA was validated by the EMA, confirming “that the application is sufficiently complete...

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