MolMed Pulls Zalmoxis Cell Therapy In EU

Company Withdraws Marketing Authorization After Failed Trial Results

The Italian biotech will redirect investment, initially reserved for Zalmoxis, to other activities that would better meet its business objectives.

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Zalmoxis Failed To Meet Its Primary Endpoint • Source: Shutterstock

Italian drug maker MolMed SPA has withdrawn the EU marketing authorization for its somatic cell therapy product, Zalmoxis, several months after an interim analysis on a Phase III trial of the product showed it to have no benefit on disease-free survival. The drug had been conditionally approved as an add-on therapy to support stem cell transplantation in patients with high-risk blood cancer. 

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