Etranacogene dezaparvovec (AMT-061 phase 2b): normal/near normal FIX activity and bleed cessation in hemophilia B

Author:

Von Drygalski Annette1,Giermasz Adam2,Castaman Giancarlo3,Key Nigel S.4ORCID,Lattimore Susan5,Leebeek Frank W. G.6,Miesbach Wolfgang7,Recht Michael5ORCID,Long Alison8,Gut Robert8,Sawyer Eileen K.8,Pipe Steven W.9ORCID

Affiliation:

1. Division of Hematology/Oncology, Department of Medicine, University of California San Diego, San Diego, CA;

2. Division of Hematology/Oncology, Department of Medicine, Hemophilia Treatment Center, University of California Davis, Sacramento, CA;

3. Careggi University Hospital, Florence, Italy;

4. Division of Hematology/Oncology, Department of Medicine, University of North Carolina, Chapel Hill, NC;

5. The Hemophilia Center, Oregon Health & Science University, Portland, OR;

6. Erasmus University Medical Center, Rotterdam, The Netherlands;

7. Department of Hemostaseology and Hemophilia Center, Medical Clinic 2, Institute of Transfusion Medicine, University Hospital Frankfurt, Frankfurt, Germany;

8. uniQure Inc, Lexington, MA; and

9. Department of Pediatrics and Pathology, University of Michigan, Ann Arbor, MI

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.

Publisher

American Society of Hematology

Subject

Hematology

Reference28 articles.

1. How to discuss gene therapy for haemophilia? A patient and physician perspective;Miesbach;Haemophilia,2019

2. Gene therapy with adeno-associated virus vector 5-human factor IX in adults with hemophilia B;Miesbach;Blood,2018

3. Adenovirus-associated virus vector-mediated gene transfer in hemophilia B;Nathwani;N Engl J Med,2011

4. Long-term safety and efficacy of factor IX gene therapy in hemophilia B;Nathwani;N Engl J Med,2014

5. Hemophilia B gene therapy with a high-specific-activity factor IX variant;George;N Engl J Med,2017

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