Tuesday June 27th 2017

FDA Approves New Dose of Copaxone To Be Taken Less Frequently

On January 28, the FDA approved a new dose of glatiramer acetate (Copaxone,® Teva Pharmaceuticals Industries, Ltd.) injected under the skin three times per week, at double the standard 20mg/mL dose, for relapsing MS. This long-approved MS disease-modifying therapy is normally taken every day. The approval was based on benefits and safety demonstrated by a company-sponsored, one-year, phase III trial comparing the higher, less-frequent dose of Copaxone with placebo.

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FDA Approves New Dose of Copaxone To Be Taken Less Frequently

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