US2009123493A1PendingUtilityA1
Composition Comprising a Colloidal Synthetic Bioresorbable Vector and a Viral Vector
Est. expiryNov 14, 2025(expired)· nominal 20-yr term from priority
A61K 47/6927A61K 2039/57A61K 39/39A61K 2039/55511C12N 2710/10343A61P 37/04A61K 39/12C12N 2740/16034A61K 2039/54A61K 2039/55583A61K 2039/523A61K 2039/543A61K 47/593A61K 47/6905C12N 2710/24143A61P 35/00C12N 2740/16234A61K 2039/53A61K 2039/5254A61K 39/21A61K 2039/6093A61K 2039/6087A61K 2039/55555A61K 2039/5256C12N 2740/16071A61K 39/235A61P 31/12C12N 7/00A61K 2039/545C12N 2710/10071A61K 47/34C12N 2710/24141C12N 2710/24171A61K 2039/55505A61K 2039/575A61K 39/285C12N 2710/10041A61K 47/6921A61K 39/0011A61K 39/00
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Claims
Abstract
The invention relates to pharmaceutical compositions containing a colloidal synthetic bioresorbable vector which comprises at least one type of proteinic substance, to a viral vector corresponding to at least one type of proteinic substance of the synthetic vector and to a method for the prophylactic, therapeutic and diagnosis use thereof.
Claims
exact text as granted — not AI-modified1 . Pharmaceutical composition comprising
a colloidal synthetic bioresorbable vector comprising at least one protein substance, and a viral vector comprising at least one nucleotide sequence which codes for a protein substance corresponding to at least one protein substance of the synthetic vector.
2 . Composition according to claim 1 , wherein it comprises a vector of spherical nature as the colloidal synthetic vector.
3 . Composition according to claim 1 , wherein the colloidal synthetic vector is prepared from at least one polymer chosen from amongst the poly(α-hydroxy acids).
4 . Composition according to claim 1 , wherein the colloidal synthetic vector is prepared from at least one natural polymer.
5 . Composition according to claim 1 , wherein the colloidal synthetic vector comprises protein substances of different types, each constituting an antigen associated with the same disease.
6 . Composition according to the claim 1 , wherein it comprises an adenovirus or a poxvirus as the viral vector.
7 . Composition according to claim 6 , wherein the poxvirus is the Modified Vaccinia Virus Ankara.
8 . Composition according to claim 1 , wherein the protein substances are of viral origin.
9 . Composition according to claim 8 , wherein the protein substances of viral origin are proteins of the HIV virus.
10 . Composition according to claim 1 , wherein the protein substance is an antigen associated with tumours.
11 . A method for preparing a medicament, comprising:
utilizing the composition of claim 1 .
12 . A method for preparing a vaccine, comprising:
utilizing the composition of claim 1 .
13 . A method for diagnosing in vitro of the pathological state for which the protein substance or substances of the synthetic vector a constitute antigens, comprising:
utilizing the composition of claim 1 .
14 . The method according to claim 13 , wherein the pathological state is a viral infection.
15 . The method according to claim 13 , wherein the pathological state is a cancer.
16 . Method of prophylactic or therapeutic treatment, in particular vaccination, comprising the administration to a patient of an effective dose of the composition as defined in claim 1 .
17 . Method of treatment according to claim 16 , wherein the composition is administered in a staggered manner.
18 . Method of treatment according to claim 17 , wherein the synthetic vector is administered before the viral vector.Join the waitlist — get patent alerts
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