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Takedas GAMMAGARD LIQUID Approved by U.S. FDA for Adults with Chronic Inflammatory Demyelinating Polyneuropathy CIDP

Takeda TSE4502NYSETAK today announced that the U.S. Food and Drug Administration FDA has approved GAMMAGARD LIQUID Immune Globulin Infusion Human 10 solution as an intravenous immunoglobulin IVIG therapy to improve neuromuscular disability and impairment in adults with chronic inflammatory demyelinating polyneuropathy CIDP. ....

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Takeda's GAMMAGARD LIQUID® Approved by U.S. FDA for Adults with Chronic Inflammatory Demyelinating Polyneuropathy (CIDP)

Takeda's GAMMAGARD LIQUID® Approved by U.S. FDA for Adults with Chronic Inflammatory Demyelinating Polyneuropathy (CIDP)
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United States , Lauren Padovan , Mamatha Pasnoor , Richard Ascroft , Demyelinating Polyneuropathy , International Media , European Medicines Agency , Department Of Neurology , Foundation International , Takeda Pharmaceutical Company Limited , University Of Kansas Medical Center , Takeda Pharmaceutical Company , Exchange Commission , Drug Administration , New Indication Delivers , Diverse Immunoglobulin , People Living , Study Data Demonstrating Safety , Intravenous Therapy , Only Intravenous , Multiple Neuromuscular Disorder Indications , Derived Therapies Business , Rasch Built Overall Disability Scale , Kansas Medical , Recombinant Human Hyaluronidase , Inflammatory Neuropathy Cause ,

Takeda's GAMMAGARD LIQUID® Approved by U.S. FDA for Adults with Chronic Inflammatory Demyelinating Polyneuropathy (CIDP)

Takeda's GAMMAGARD LIQUID® Approved by U.S. FDA for Adults with Chronic Inflammatory Demyelinating Polyneuropathy (CIDP)
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