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Etranacogene dezaparvovec (AMT-061 phase 2b): normal/near normal FIX activity and bleed cessation in hemophilia B.
Von Drygalski, Annette; Giermasz, Adam; Castaman, Giancarlo; Key, Nigel S; Lattimore, Susan; Leebeek, Frank W G; Miesbach, Wolfgang; Recht, Michael; Long, Alison; Gut, Robert; Sawyer, Eileen K; Pipe, Steven W.
Afiliación
  • Von Drygalski A; Division of Hematology/Oncology, Department of Medicine, University of California San Diego, San Diego, CA.
  • Giermasz A; Division of Hematology/Oncology, Department of Medicine, Hemophilia Treatment Center, University of California Davis, Sacramento, CA.
  • Castaman G; Careggi University Hospital, Florence, Italy.
  • Key NS; Division of Hematology/Oncology, Department of Medicine, University of North Carolina, Chapel Hill, NC.
  • Lattimore S; The Hemophilia Center, Oregon Health & Science University, Portland, OR.
  • Leebeek FWG; Erasmus University Medical Center, Rotterdam, The Netherlands.
  • Miesbach W; Department of Hemostaseology and Hemophilia Center, Medical Clinic 2, Institute of Transfusion Medicine, University Hospital Frankfurt, Frankfurt, Germany.
  • Recht M; The Hemophilia Center, Oregon Health & Science University, Portland, OR.
  • Long A; uniQure Inc, Lexington, MA; and.
  • Gut R; uniQure Inc, Lexington, MA; and.
  • Sawyer EK; uniQure Inc, Lexington, MA; and.
  • Pipe SW; Department of Pediatrics and Pathology, University of Michigan, Ann Arbor, MI.
Blood Adv ; 3(21): 3241-3247, 2019 11 12.
Article en En | MEDLINE | ID: mdl-31698454
ABSTRACT
Etranacogene dezaparvovec (AMT-061) is a recombinant AAV5 vector including a gene cassette containing the factor IX (FIX) Padua variant under the control of a liver-specific promoter. A phase 2b study was conducted to confirm that a single dose of 2 × 1013 genome copies per kilogram of etranacogene dezaparvovec will result in FIX activity ≥5% 6 weeks after dosing. Secondary end points included FIX activity at other time points, bleed frequency, FIX replacement, and safety. Etranacogene dezaparvovec was administered as a single IV infusion to 3 adults with severe to moderately severe hemophilia B. Before treatment, participants had low levels of preexisting neutralizing antibodies to AAV5. This article reports a planned 26-week interim assessment. At week 6, mean FIX activity was 31% (23.9%-37.8%), increasing to 47% (33.2%-57.0%) at 26 weeks, with 2 subjects exhibiting sustained activity >40%. Consistent with the FIX activity, etranacogene dezaparvovec was associated with a complete bleed cessation with no need for FIX replacement therapy up to 26 weeks. Etranacogene dezaparvovec was generally well tolerated. No clinically significant elevations in levels of liver enzymes or inflammatory markers were observed, and no use of corticosteroids related to treatment was required. In individuals with severe to moderately severe hemophilia B, etranacogene dezaparvovec resulted in clinically relevant increases in FIX activity, cessation of bleeds, and abrogation of the need for FIX replacement, despite the presence of preexisting anti-AAV5 neutralizing antibodies detected by using a highly sensitive luciferase assay. Consistency of results in the 3 participants supported an expanded evaluation of the safety/efficacy of etranacogene dezaparvovec in the HOPE-B (Health Outcomes With Padua Gene; Evaluation in Hemophilia-B) phase 3 trial. The current trial was registered at www.clinicaltrials.gov as #NCT03489291.

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Blood Adv Año: 2019 Tipo del documento: Article País de afiliación: Canadá

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Blood Adv Año: 2019 Tipo del documento: Article País de afiliación: Canadá