Study title:
A multi-center, randomized, double-blind, placebo-controlled Phase I/II trial to compare the safety, tolerability and immunogenicity of the therapeutic THV01 vaccination of HIV-1 clade B infected patients under highly antiretroviral therapy
EU record number:
B/BE/12/BVW1
EudraCT number:
2011-006260-52
Pharmaceutical study code:
THV01-11-1
Company / Sponsor:
TheraVectys
Phase:
I
Treated organism:
Humans
Indication category:
Infectious disease
Disease:
AIDS
Therapeutic approach:
Immunotherapy
Genetic modification:
genes encoding the epitopes of the HIV-1 Gag, Pol and Nef proteins
Method of transfer of nucleic acid of interest:
Human immunodeficiency virus (HIV): NL4-3 strain of HIV-1
Administered biological material:
non replication comptent lentivirus
Route of administration:
intramuscular
Locations in Belgium:
CHU Liège, CHU St Pierre Brussels
Nr of subjects:
36
Foreseen duration:
1 year
Type of procedure:
Contained use and Deliberate release
Current status:
Authorized
Information for the public
Information related to the decision procedure
-
18 October 2012: The Federal Minister gives a final decision (positive with conditions) for this trial.
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11 September 2012: The Biosafety Advisory Council issues a positive advice (with conditions) for this trial.