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Panel to Discuss Hoffmann-La Roche’s Actemra

06/05/2008

Federal Register Notice: FDA’s Arthritis Advisory Committee will meet 7/29, from 8:30 a.m. to 3:30 p.m. at the Hilton Washington DC/Silver Spring, The Ballrooms, 8727 Colesville Rd., Silver Spring, MD. Contact Nicole Vesely, (301) 827-6793. The committee will discuss Hoffmann-La Roche, Inc.’s BLA for Actemra (tocilizumab), for treating adult patients with moderately to severely active rheumatoid arthritis. To view this notice, click here.

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