IP Library Granted Patent US 10,166,272
Granted Patent B2
US 10,166,272 · App. 15/321,416 · Granted Jan 1, 2019

Efficient systemic treatment of dystrophic muscle pathologies

Inventors: George Dickson (London, GB); Thomas Voit (Boullay les Troux, FR); Philippe Moullier (Nantes, FR); Caroline Le Guiner (Granchamp des Fontaines, FR)
Assignees: GENETHON; ROYAL HOLLOWAY AND BEDFORD NEW COLLEGE
A61K38/1719A61K48/005A61K48/0058A61K48/0075C12N7/00C12N15/86C12N2750/14132C12N2750/14143C12N2750/14171C12N2840/007
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Quick Facts
Patent No.
US 10,166,272
App. No.
15/321,416
Granted
Jan 1, 2019
Kind
B2
Abstract

A composition comprising a gene therapy product for use in the treatment of a dystrophic disease in a subject, advantageously in humans, wherein: —the gene therapy product comprises a nucleic acid sequence encoding a functional microdystrophin; —the composition is systemically administered.

Claims (13)

1. A method of treating Duchenne muscular dystrophy (DMD) in a human, comprising:

systemically administering by intravascular injection to a human in need thereof a gene therapy product that comprises an adeno-associated viral (AAV) vector of serotype 8 or 9 which harbors a nucleic acid sequence encoding a human ΔR4-R23/ΔCT microdystrophin, thereby treating DMD in the human.

2. The method according to claim 1 , wherein the nucleic acid sequence comprises SEQ ID NO: 1.

3. The method according to claim 1 , wherein the AAV vector is an AAV8 vector or an AAV2/8 vector.

4. The method according to claim 1 , wherein the gene therapy product is administered with a dose less than or equal to 10 15 vg/kg.

5. The method according to claim 4 , wherein the gene therapy product is administered with a dose between 10 12 vg/kg and 10 14 vg/kg.

6. The method according to claim 1 , wherein the gene therapy product is systemically administered once.

7. The method according to claim 1 , wherein the method ameliorates the muscular function of the human.

8. The method according to claim 1 , wherein the method ameliorates the cardiac function of the human.

9. The method according to claim 1 , wherein the method ameliorates the respiratory function of the human.

10. The method according to claim 1 , wherein the gene therapy product is administered by intravenous injection.

11. The method according to claim 1 , wherein the administration of the gene therapy product does not induce an adverse immune response in the human.

12. The method according to claim 1 , wherein the nucleic acid sequence comprises nucleotides 215 to 4353 of SEQ ID NO: 1.

Assignments (4)
MERGER Recorded Sep 7, 2023
From: UNIVERSITE DE NANTES
To: NANTES UNIVERSITE
Reel/Frame 064824/0596 →
CORRECTIVE ASSIGNMENT TO CORRECT THE ADDRESS IN THE SIXTH ASSIGNEE AND CLEARER VERSIONS OF PAGES 3 AND 12 PREVIOUSLY RECORDED AT REEL: 058242 FRAME: 0262. ASSIGNOR(S) HEREBY CONFIRMS THE ASSIGNMENT. Recorded Mar 30, 2022
From: GENETHON; ROYAL HOLLOWAY AND BEDFORD NEW COLLEGE
To: ASSOCIATION INSTITUT DE MYOLOGIE; INSTITUT NATIONAL DE LA SANTE ET DE LA RECHERCHE MEDICALE; CENTRE NATIONAL DE LA RECHERCHE SCIENTIFIQUE; SORBONNE UNIVERSITE; CENTRE HOSPITALIER UNIVERSITAIRE DE NANTES; UNIVERSITE DE NANTES
Reel/Frame 059658/0764 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Nov 30, 2021
From: GENETHON; ROYAL HOLLOWAY AND BEDFORD NEW COLLEGE
To: ASSOCIATION INSTITUT DE MYOLOGIE; INSTITUT NATIONAL DE LA SANTE ET DE LA RECHERCHE MEDICALE; CENTRE NATIONAL DE LA RECHERCHE SCIENTIFIQUE; SORBONNE UNIVERSITE; CENTRE HOSPITALIER UNIVERSITAIRE DE NANTES; UNIVERSITE DE NANTES
Reel/Frame 058242/0262 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 18, 2017
From: DICKSON, GEORGE; VOIT, THOMAS; MOULLIER, PHILIPPE; LE GUINER, CAROLINE
To: GENETHON; ROYAL HOLLOWAY AND BEDFORD NEW COLLEGE
Reel/Frame 041010/0652 →
Priority Claims (1)
EP 14174848 · Jun 27, 2014 · regional
Continuity (1)
Related Publication 20170157213A1 · Jun 8, 2017
Cited By (6)
US 12,257,317 US 12,421,285 US 12,491,265 US 12,653,909 US 12,680,108 US 12,697,399