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MedImmune Announces Phase 2 Safety Data for Anti-RSV Antibody and National RSV Surveillance Results
Date:10/4/2007

irology Laboratory, Universidad Catolica de Chile,

-- Friday, October 5, 2007; 12:30 - 2:00 p.m. in Poster Halls G-H.

-- This study assessed the safety and immunogenicity of

motavizumab, an investigational anti-RSV MAb, in young children

with a history of prematurity who received two sequential

seasons of the antibody.

RSV Surveillance: Retrospective and Current Data on the Variance in Season Onsets and Offsets (Poster Presentation #719) - Jessie R. Groothuis M.D., MedImmune,

-- Saturday, October 6, 2007; 12:15 - 1:45 p.m. in Poster Halls G-H.

-- A nationwide active surveillance program was established to

evaluate the variability of the RSV season temporally and

geographically in the United States. Laboratory results from a

three-year period were analyzed by month and by geographic

region.

Additional information regarding the IDSA 45TH Annual Meeting can be found at http://www.idsociety.org/Meetingshome.aspx?id=238 .

MedImmune's Commitment to RSV Prevention

MedImmune is a world leader in the development of innovative therapeutic biologic products to prevent RSV disease. In 1996, MedImmune launched the first anti-RSV drug, RespiGam(R) (respiratory syncytial virus immune globulin intravenous (human) (RSV-IGIV)), which was a polyclonal antibody administered via four-hour intravenous infusion. In 1998, MedImmune introduced Synagis(R) (palivizumab), which was the first MAb to receive U.S. Food and Drug Administration (FDA) approval for an infectious disease. With the development of motavizumab, MedImmune continues to reinforce its commitment to developing anti-RSV products. In a head-to-head comparative Phase 3 trial with Synagis, motavizumab met its primary endpoint of reducing RSV-related hospitalizations in high-risk pe
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SOURCE MedImmune, Inc.
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