uniQure schedules FDA meeting to discuss accelerated approval of HD therapy
🔹 Key message
uniQure is planning an official discussion with the US Food and Drug Administration (FDA) to accelerated approval for its gene therapy AMT-130 for the treatment of Huntington's disease for the treatment of Huntington's disease.
🔍 Details
- The company is preparing for a pre-BLA meeting with the FDA (BLA = Biologics License Application).
- The aim is to bring the therapy bring the therapy to market more quicklyas Huntington's disease is a a rare, fatal neurodegenerative disease. disease.
- uniQure sees positive clinical data as the basis for the application for accelerated approval
📈 Market impact
- The news has caused uniQure's share price to rise significantly.
- Investors see this as a potential turning point for the company.
🧠 Background to AMT-130
- AMT-130 is a unique gene therapythat targets the cause of Huntington's disease.
- The therapy utilizes AAV vectorsto deliver a gene into the central nervous system.


