A European and Canadian multicenter, randomized, double-blind, placebo controlled study to evaluate the efficacy and safety of Ad5FGF-4 in patients with stable angina

Date receipt dossier

Company / Sponsor

Schering N.V./S.A.

Phase

IIb/III

Treated organism

Humans

Indication category

Cardiovascular therapy

Disease

Chronic angina pectoris

Therapeutic approach

Gene therapy

Genetic modification

human FGF-4

Method of transfer of nucleic acid of interest

Human Adenovirus serotype 5

Administered biological material

Recombinant Adenovirus D (E1A, E1B)

Route of administration

Intracoronary

Locations in Belgium

Universitair Ziekenhuis Gasthuisberg, Leuven - O.-L.-Vrouwziekenhuis, Aalst

Type of procedure

Contained use only

Current status

Authorized

Pharmaceutical study code

305602

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