FDA and Celgene Revlimid Briefing Documents for Advisory Committee Meeting Available Online
13th Sep 2005, 17:17 GMT
Celgene Corp announced that the Oncologic Drugs Advisory Committee of the US FDA has posted on its website briefing documents for the ODAC meeting scheduled to review the REVLIMID New Drug Application seeking approval for REVLIMID for the treatment of patients with transfusion-dependent anemia due to low- or intermediate-1-risk myelodysplastic syndromes associated with a deletion 5q cytogenetic abnormality with or without additional cytogenetic abnormalities.
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