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Data Presented at the American Academy of Neurology's Annual,Meeting Provide Update on Utilization and Safety of Tysabri in,Patients with Multiple Sclerosis

actual results to differ materially from the companies' current expectations include the risk that we may be unable to adequately address concerns or questions raised by FDA or other regulatory authorities, that concerns may arise from additional data, that the incidence and/or risk of PML or other opportunistic infections in patients treated with TYSABRI may be higher than observed in clinical trials, or that the companies may encounter other unexpected hurdles. Drug development and commercialization involves a high degree of risk.

For more detailed information on the risks and uncertainties associated with the companies' drug development and other activities, see the periodic and current reports that Biogen Idec and Elan have filed with the Securities and Exchange Commission. The companies assume no obligation to update any forward-looking statements, whether as a result of new information, future events or otherwise.

Contact

Media Contacts:
Biogen Idec
Amy Brockelman, 617 914 6524
or
Elan
Matt Dallas, 212 850 5664
Elizabeth Headon, 353 1 498 0300
or
Investor Contacts:
Biogen Idec
Eric Hoffman, 617 679 2812
or
Elan
Chris Burns, 353 1 709 4444
800 252 3526


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