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ELN » Topics » Redosing of Tysabri in Clinical Trial

This excerpt taken from the ELN 20-F filed Mar 30, 2006.
Redosing of Tysabri in Clinical Trial
 
On February 15, 2006, Elan and Biogen Idec were informed by the FDA that it had removed the hold on clinical trial dosing of Tysabri in MS in the United States, and the companies announced that they expected to begin an open label, multi-center safety extension study of Tysabri monotherapy in the United States and internationally.
 
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