Press Release Source: Biogen Idec; Elan Corporation, plc
Monday June 5, 2:57 pm ET
The FDA granted approval for reintroduction based on the review of TYSABRI clinical trial data; revised labeling with enhanced safety warnings; and a risk management plan (TOUCH Prescribing Program) designed to inform physicians and patients of the benefits and risks of TYSABRI treatment and minimize potential risk of progressive multifocal leukoencephalopathy (PML). Because of the increased the risk of PML, TYSABRI monotherapy is generally recommended for patients who have had an inadequate response to, or are unable to tolerate, alternate MS therapies.
SATELLITE FEEDS:
Monday, June 5th, 2006 Monday, June 5th, 2006
3:30 PM - 3:45 PM ET 6:15 PM - 6:30 PM ET
IA 6 IA 6
Transponder 15 Transponder 16
C-Band C-Band
Downlink: 4000 Vertical Downlink: 4020 Horizontal
Tuesday, June 6th, 2006
3:00 AM - 3:15 AM ET
IA 6
Transponder 15
C-Band
Downlink: 4000 Vertical
Preview and access this video on Pathfire DMG: 24030
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FORMAT: News Package With Extra Soundbites and B-roll.
NEWS: FDA Approves Reintroduction of TYSABRI® For Relapsing Forms of Multiple Sclerosis
ADDITIONAL RESOURCES: Video, contact information and more available at http://www.prnewswire.com/broadcast/24030/consumer.shtml.
SOUNDBITES:
* Sonda Lawson, Director of MS Clinical Research and Services at The
Michigan Institute for Neurological Disorders, Patient
* Howard Rossman, M.D., Medical Director of the Michigan Institute For
Neurological Disorders
* Celeste Markey, MS Patient
B-ROLL INCLUDES: ***TYSABRI Infusion Footage***Patient Lifestyle Footage***Clinic Examination Footage***Product Shot***
VIDEO PROVIDED BY: Biogen Idec and Elan
Source: Biogen Idec; Elan Corporation, plc
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