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uniQure — Third Quarter 2026 Earnings Summary

  • Revenue increased to $5.2 million from $3.7 million year-over-year, driven by higher license revenue, while the net loss narrowed to $61.2 million ($0.88 per share) from $80.5 million ($1.38 per share) in the prior year period.
  • The FDA granted Priority Review for the BLA of ifezuntirgene inilparvovec (AMT-130) for Huntington's disease, setting a PDUFA target action date of May 1, 2027, with U.S. patient screening for the required confirmatory study expected to begin by the end of 2026.
  • Cash, cash equivalents, and investment securities rose to $768.4 million as of September 30, 2026, providing sufficient funding to cover operating expenses through 2030.
  • The U.K. MHRA validated the Marketing Authorization Application for AMT-130, and the company resumed enrollment for the AMT-191 Fabry disease study in August 2026 following the resolution of prior safety pauses.
Company
UNIQURE NV
Sector
Healthcare
Industry
Biotechnology