Study title:
Phase III trial investigating a AAV vector containing a variant of human factor IX gene administered to adult subjects with severe or moderately-severe hemophilia B
Long title:
Phase III, open-label, single-dose, multi-centre multinational trial investigating a serotype 5 adeno-associated viral vector containing the Padua variant of a codon-optimized human factor IX gene (AAV5-hFIXco-Padua, AMT-061) administered to adult subjects with severe or moderately-severe hemophilia B
Date receipt dossier:
12 oct 2018
EU record number:
B/BE/18/BVW7
EudraCT number:
2017-004305-40
Company / Sponsor:
uniQure biopharma B.V.
Phase:
III
Treated organism:
Humans
Indication category:
Genetic disorders
Disease:
Hemophilia B
Therapeutic approach:
Gene therapy
Genetic modification:
Recombinant adeno associated viral vector containing the wild type modified to express the Padua derivative of human coagulation factor IX cDNA
Method of transfer of nucleic acid of interest:
Replication competent adeno-associated viral vector
Administered biological material:
Recombinant virus
Route of administration:
Intravenous
Locations in Belgium:
UZ Leuven; Cliniques Universitaires Saint-Luc (Brussels)
Nr of subjects:
56
Foreseen duration:
Q1-2019 until Q4-2021
Type of procedure:
Contained use and Deliberate release
Current status:
Authorized
Information for the public
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Public information presented according to the provisions of Directive 2001/18/EC
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Information related to the decision procedure
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11 December 2018 - The Biosafety Advisory Council issues a positive advice (with conditions) for this trial
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18 January 2019: The Federal Ministers give a final decision (positive) for this trial