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uniQure запланировала встречу типа A с FDA для обсуждения пакета данных BLA по AMT-130 — своей экспериментальной генной терапии болезни Гентингтона. Встреча предназначена для обсуждения пути ускоренного одобрения. Компания предоставит обновление по регуляторным вопросам после получения официальных протоколов встречи.
EX-99.1 2 qure-20260109xex99d1.htm EX-99.1 Exhibit 99.1 uniQure Announces Type A Meeting Scheduled with FDA Lexington, MA and Amsterdam, the Netherlands, January 9, 2026 — uniQure N.V. (NASDAQ: QURE), a leading gene therapy company advancing transformative therapies for patients with severe medical needs, today announced a Type A meeting with the U.S. Food and Drug Administration (FDA) has been scheduled to discuss the Biologics License Application (BLA) data package to support accelerated approval of AMT-130, the Company’s investigational gene therapy for the treatment of Huntington’s disease. “We look forward to a constructive discussion with the FDA as we work toward a timely resolution regarding an accelerated approval pathway for AMT-130,” said Matt Kapusta, chief executive off