Celltrion To Jostle For Space In Crowded EU Bevacizumab Market

As Celltrion Also Submits Phase III Interchangeable Humira Data

The European Commission has approved Vegzelma, a bevacizumab biosimilar developed by South Korean biopharma giant Celltrion. Vegzelma joins nine other bevacizumab biosimilar marketing authorization applications approved in the EU, promising to intensify price competition for the  critical late-stage cancer treatment.

EU Flag Eye Close-Up
Celltrion is eyeing opportunity in the EU bevacizumab market • Source: Shutterstock

Celltrion has received final approval from the European Commission for its Vegzelma bevacizumab biosimilar to Roche’s Avastin. Bevacizumab is a tumor-targeting humanized monoclonal antibody designed for intravenous delivery.

Vegzelma is indicated for a range of oncology indications, including metastatic breast cancer, non-small cell lung cancer, advanced and/or metastatic...

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