Study title:
GenePHIT: A study to learn more about how well a new gene therapy (AB-1002) works and its safety in participants with congestive heart failure
Long title:
A phase 2, adaptive, double-blinded, placebo controlled, randomized, multi-center trial to evaluate the efficacy, safety and tolerability of intracoronary infusion of AB-1002 in adult subjects with New York Heart Association (NYHA) Class III heart failure and non-ischemic cardiomyopathy
Date receipt dossier:
11 jul 2025
EU record number:
B/BE/25/BVW5
EudraCT number:
2024-510581-17-00
Company / Sponsor:
Asklepios BioPharmaceutical (AskBio)
Phase:
II
Treated organism:
Humans
Indication category:
Congestive Heart failure
Disease:
NYHA Class III heart failure and non-ischemic cardiomyopathy
Therapeutic approach:
Gene therapy
Genetic modification:
Non-replicating recombinant vector derived from adeno-associated virus AAV2i8 carrying the transgene encoding for the human activated Inhibitor-1c ( I-1c)
Method of transfer of nucleic acid of interest:
Non-replicating recombinant vector derived from adeno-associated virus AAV2/AAV8
Administered biological material:
Genetically modified virus
Route of administration:
Intracoronary
Locations in Belgium:
AZORG in Aalst
UZ Antwerpen in Edegem
UZ Gent in Gent
AZ Delta in Roeselare
Nr of subjects:
Up to 150 patients overall and 5 patients in Belgium
Foreseen duration:
from Aug.2025 till 31.12.2030
Type of procedure:
Contained use and Deliberate release
Current status:
Under evaluation
Information for the public
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Public information according to the provisions of Directive 2001/18/EC