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Celgene granted EU approval to market myeloma drug

Celgene International Sarl has announced that Thalidomide Pharmion has received full marketing authorization from the European Commission for use in combination with melphalan and prednisone as a treatment for patients with newly diagnosed multiple myeloma.

Aart Brouwer, president of Celgene International, said: “We are working diligently with local regulatory authorities to determine next steps for pricing, reimbursement and distribution plans for all EU member states so that Thalidomide Pharmion will be available for eligible patients as quickly as possible.”