FDA Under Pressure to Approve UniQure's Huntington's Treatment Amid Advocacy Groups' Plea
ByAinvest
Monday, Jan 26, 2026 6:09 am ET1min read
QURE--
Patient advocates for Huntington's disease are urging the FDA to approve UniQure's gene therapy, citing a clinical trial that showed patients progressed 75% slower than a comparison group. The FDA had previously agreed that the trial's results were sufficient for approval but has since changed its stance. The outcome will provide insight into the FDA's flexibility with new treatments for rare diseases.

Stay ahead of the market.
Get curated U.S. market news, insights and key dates delivered to your inbox.
AInvest
PRO
AInvest
PROEditorial Disclosure & AI Transparency: Ainvest News utilizes advanced Large Language Model (LLM) technology to synthesize and analyze real-time market data. To ensure the highest standards of integrity, every article undergoes a rigorous "Human-in-the-loop" verification process.
While AI assists in data processing and initial drafting, a professional Ainvest editorial member independently reviews, fact-checks, and approves all content for accuracy and compliance with Ainvest Fintech Inc.’s editorial standards. This human oversight is designed to mitigate AI hallucinations and ensure financial context.
Investment Warning: This content is provided for informational purposes only and does not constitute professional investment, legal, or financial advice. Markets involve inherent risks. Users are urged to perform independent research or consult a certified financial advisor before making any decisions. Ainvest Fintech Inc. disclaims all liability for actions taken based on this information. Found an error?Report an Issue

Comments
No comments yet