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VisitVyvgart Hytrulo EMA approval for CIDP by end of 2024?
Yes • 50%
No • 50%
Official announcement from the European Medicines Agency (EMA) or Argenx's press release
Argenx's Vyvgart Hytrulo Shot Gains Second FDA Approval for CIDP with Halozyme's ENHANZE
Jun 21, 2024, 09:10 PM
Argenx's Vyvgart Hytrulo shot has received its second US FDA approval to treat Chronic Inflammatory Demyelinating Polyneuropathy (CIDP), a rare nervous system disorder. This approval marks a significant milestone for the biotechnology firm, which has faced a series of setbacks. The Vyvgart Hytrulo shot is co-formulated with Halozyme's ENHANZE technology. This label expansion into CIDP adds to Argenx's growth prospects ahead of more clinical milestones anticipated in 2024.
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Approval • 33%
Conditional Approval • 33%
Rejection • 34%
Yes • 50%
No • 50%
Stock price decreases by over 20% • 33%
Stock price remains within 20% of current value • 34%
Stock price increases by over 50% • 33%
Phase II success for new indication • 33%
Phase III success for current indications • 33%
New FDA approval for different indication • 34%