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Search the database for deliberate release of GM medicinal products
Displaying 1 - 3 of 3
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EU record number
Title
Company / Sponsor
Treated organism
Genetic modification
B/BE/26/BVW3
A phase I/II/III study with a dose determination part followed by an efficacy and safety evaluation, quadruple blind placebo-controlled part and then by a long-term safety follow up part, in ambulant boys with Duchenne Muscular Dystrophy
GENETHON
Humans
Non-replicating recombinant vector derived from adeno-associated virus AAV, lacking all AAV viral genes and carrying the human dystrophin (hMD1) gene
MB-CART2019.1
A phase I/II safety, dose finding and feasibility trial of MB-CART2019.1 in patients with relapsed or resistant B-NHL
Miltenyi Biotech GmbH
Humans
CD19 and CD20 chimeric antigen receptor
Only notified under the "contained use" procedure. Dossier submitted on
8 July, 2010
.
An open-label, phase I, dose-escalation and safety study of two intramuscular injections at dose of 2.9 log or 4 log CCID50 of the recombinant HIV I clade B measles vaccine vector in healthy adults.
Institut Pasteur - Paris
Humans
Gag, Pol, Nef genes of HIV
