Reports 2022 revenue $106.48M, consensus $30.57M. "We had a strong ending to 2022 with the historic approval of the world’s first gene therapy for hemophilia B for which we led the multi-year research and clinical development, and through our partnership with CSL Behring, HEMGENIX will now be available to patients in the United States and European Union," stated Matt Kapusta, chief executive officer of uniQure. "We are immensely proud of our efforts that led to this product approval, and of the innovation and leadership in genomic medicine that it represents. At the same time, we are working with urgency to advance AMT-130, the first AAV gene therapy being clinically investigated in Huntington’s disease, and are on track to provide a clinical update from our U.S. Phase I/II study in the second quarter of 2023. We are also preparing for the initiation of two new Phase I/II studies in refractory temporal lobe epilepsy and SOD1-ALS in the second half of this year, and readying for the submission of an investigational new drug application in Fabry disease in 2023. Throughout this progress, we have established cutting-edge capabilities in the field of genetic medicines – from how we discover and develop our gene therapies, to how we successfully navigate complex clinical and regulatory pathways, to how we manufacture these novel gene therapies globally for clinical and commercial usage," said Mr. Kapusta. "We believe these capabilities position us well for continued growth and success as we look forward to developing more life-altering gene therapy products for patients in need."
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- uniQure Announces 2022 Financial Results and Highlights Recent Company Progress
- uniQure announces HOPE-B trial published in NEJM
- uniQure Announces HOPE-B Clinical Trial Data Published in the New England Journal of Medicine, Demonstrating Durability and Other Benefits of HEMGENIX® (etranacogene dezaparvovec-drlb)
- uniQure announces CMA from European Commission for HEMGENIX
- uniQure announces the European Commission approval of the first gene therapy for adults with hemophilia B