Takeda's GAMMAGARD LIQUID Approved By FDA For Adults with Chronic Inflammatory Demyelinating Polyneuropathy
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The FDA has approved Takeda's GAMMAGARD LIQUID for adults with Chronic Inflammatory Demyelinating Polyneuropathy (CIDP). This approval is based on Phase 3 ADVANCE-CIDP study data, which demonstrated the safety and efficacy of GAMMAGARD LIQUID as an intravenous therapy. With this new indication, GAMMAGARD LIQUID becomes the only intravenous immune globulin (IVIG) approved for multiple neuromuscular disorder indications in the U.S.
January 29, 2024 | 4:11 pm
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Takeda's GAMMAGARD LIQUID has been approved by the FDA for the treatment of CIDP, potentially increasing the drug's market and enhancing Takeda's immunoglobulin portfolio.
FDA approvals typically lead to increased market opportunities and can positively influence a company's stock price in the short term. The approval of GAMMAGARD LIQUID for a new indication enhances Takeda's product offering and may lead to increased sales and revenue, which is likely to be viewed favorably by investors.
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