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Will UniQure's AMT-130 receive FDA approval for Huntington’s disease by end of 2024?
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Resolution / Starting Odds
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FDA announcements and UniQure press releases
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UniQure Stock Surges 60% on Positive AMT-130 Huntington’s Gene Therapy Data
Jul 9, 2024, 02:51 PM
UniQure has announced positive interim data from its Phase I/II trials of AMT-130, a gene therapy for Huntington’s disease. The data demonstrated a statistically significant, dose-dependent slowing of disease progression, with patients receiving high-dose AMT-130 showing an 80% reduction in the progression of the disease in the composite Unified Huntington’s measure. Following this announcement, uniQure's stock surged by 60%, reflecting investor optimism about the potential of this one-time therapy. The stock saw a pre-market increase of 27% and continued to rise throughout the day.
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Less than 50% efficacy • 25%
50-69% efficacy • 25%
70-89% efficacy • 25%
90% or higher efficacy • 25%
FDA • 33%
EMA • 33%
Both • 34%
Phase III trial initiation • 25%
FDA accelerated approval • 25%
New interim data release • 25%
Other milestone • 25%
Full Approval • 25%
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Conditional Approval • 25%
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