ImClone Systems Inc and Bristol-Myers Squibb Co said the US Food and Drug
Administration has given priority review of a supplemental biologics license application for their anti-cancer drug Erbitux.
The companies said through the application, they aim to include evidence of improved overall survival in the product's labelling in the third-line treatment of patients with metastatic colorectal cancer.
They said the FDA aims to announce the results of review in early October.
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source:www.forbes.com
Monday, June 11, 2007
Bristol-Myers, ImClone say FDA grants priority review of cancer drug
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