FIELD: medicine, pharmaceutics.
SUBSTANCE: group of inventions refers to medicine, and concerns a pharmaceutical composition for the therapy of neurodegenerative disorders, particularly amyotrophic lateral sclerosis, containing an effective amount of an adenoviral vector in the form of a non-replicating nanoparticle of a human adenovirus serotype 5 genome with an insert of human angiogenin gene producing angiogenin and the non-replicating nanoparticles of the human adenovirus serotype 5 genome with an insert of a vascular endothelial growth factor gene producing the vascular endothelial growth factor in the human body, wherein the human angiogenin gene and the human vascular endothelial growth factor gene are cloned in two expression cassettes of one non-replicating nanoparticles of the human adenovirus serotype 5 genome, a method of treating amyotrophic lateral sclerosis implying administering a therapeutically effective dose of the above pharmaceutical composition.
EFFECT: group of inventions provides the higher therapeutic effectiveness and the absence of undesired side effects in the patients.
19 cl, 7 ex, 4 dwg, 2 tbl
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RU2707131C2 |
NON-INFECTIOUS FOR HUMAN ADENOVIRUS AS VECTOR FOR SUBSTITUTION GENETIC THERAPY OF ANGIOGENESIS DISORDER PROVIDING EFFECTIVE SYNTHESIS OF HUMAN ANGIOGENIN IN MAMMALIAN TRANSFECTED CELLS, METHOD FOR ANGIOGENESIS INDUCTION, METHOD FOR TREATMENT OF ISCHEMIC DISEASE, COMPOSITION FOR INDUCTION OF ANGIOGENESIS AND TREATMENT OF ISCHEMIC DISEASE | 2005 |
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Authors
Dates
2013-08-27—Published
2012-02-16—Filed