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Last updated on June 2, 2012 at 19:02 EDT

/K I L L K I L L K I L L — Celgene Corporation/

June 15, 2007
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We are advised by Celgene Corporation that journalists and other readers should disregard the news release, REVLIMID(R) Granted Full Marketing Authorization for Treatment of Multiple Myeloma in the European Union, issued earlier today over PR Newswire. The drug remains under review by EMEA and has not been approved.

Celgene Corporation

Web site: http://www.celgene.com/http://www.revlimid.com/