UniQure: Accelerated Approval Plan With US FDA May Save Five Years

Gene Therapy AMT-130 Could Become First Huntington’s Therapy

UniQure said discussions with the FDA resulted in a path forward for seeking accelerated approval of its gene therapy AMT-130 in Huntington’s disease.

Amsterdam-based uniQure is looking for accelerated approval in Huntington's disease (Shutterstock)

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