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Celgene International Sàrl, a subsidiary of Celgene Corporation
CELG, is providing a regulatory update for REVLIMID (lenalidomide) and pomalidomide as treatments for multiple myeloma.
We have decided to withdraw the new indication submission to the Committee for Medicinal Products for Human Use (CHMP) for REVLIMID (lenalidomide), which was intended for the maintenance treatment of newly diagnosed multiple myeloma patients who have not progressed following initial treatment with melphalan, prednisone and REVLIMID (lenalidomide), or maintenance therapy following autologous stem cell transplantation.
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