IP Library Granted Patent US 10,906,981
Granted Patent B2
US 10,906,981 · App. 14/906,259 · Granted Feb 2, 2021

Compositions and methods related to structures that cross the blood brain barrier

Inventors: William M. Pardridge (Pacific Palisades, CA); Ruben J. Boado (Agoura Hills, CA)
C07K16/2869C07K14/475G01N33/66C07K2317/75C07K2317/76C07K2319/00G01N2400/00G01N2800/042G01N2800/52
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Quick Facts
Patent No.
US 10,906,981
App. No.
14/906,259
Granted
Feb 2, 2021
Kind
B2
Abstract

Provided herein are compositions, kits, methods and systems related to administering a structure that crosses the blood brain barrier (BBB) along with a monosaccharide, either simultaneously or consecutively. The structure may be, for example an antibody or fusion antibody that binds to an insulin receptor.

Claims (28)

1. A method for treating a subject with a central nervous system (CNS) disorder, wherein the disorder is selected from the group consisting of Hurler's Syndrome, Hunter's Syndrome, Type I mucopolysaccharidosis, Type II mucopolysaccharidosis, and a lysosomal storage disorder, the method comprising administering to the subject:

a. a structure that binds to a receptor expressed on the blood brain barrier (BBB), wherein the structure comprises HIRMab; and

b. a glucose monosaccharide;

wherein the administering treats the subject having the CNS disorder.

2. The method of claim 1 , wherein the structure is a fusion antibody.

3. The method of claim 2 , wherein the fusion antibody binds to a receptor expressed on the BBB.

4. The method of claim 3 , wherein the receptor expressed on the BBB is an insulin receptor.

5. The method of claim 1 , wherein the structure is a fusion antibody comprising: an amino acid sequence of a heavy chain immunoglobulin covalently linked to an amino acid sequence of a polypeptide or an amino acid sequence of a light chain immunoglobulin covalently linked to an amino acid sequence of a polypeptide.

6. The method of claim 5 , wherein the polypeptide comprises an enzyme.

7. The method of claim 5 , wherein the fusion antibody acts as an agonist.

8. The method of claim 1 , wherein the glucose monosaccharide is administered to the subject after the structure is administered to the subject.

9. The method of claim 1 , wherein the structure causes hypoglycemia.

10. The method of claim 9 , wherein the glucose monosaccharide ameliorates the hypoglycemia.

11. A method for treating a subject with a central nervous system (CNS) disorder comprising administering to the subject:

a. a structure that binds to a receptor expressed on the blood brain barrier (BBB), wherein the structure comprises HIRMab and wherein the structure is a fusion antibody comprising: an amino acid sequence of a heavy chain immunoglobulin covalently linked to an amino acid sequence of a polypeptide which polypeptide comprises a lysosomal enzyme or an amino acid sequence of a light chain immunoglobulin covalently linked to an amino acid sequence of a polypeptide which polypeptide comprises a lysosomal enzyme; and

b. a glucose monosaccharide;

wherein the administering treats the subject having the CNS disorder.

12. The method of claim 11 , wherein the lysosomal enzyme is selected from the group consisting of: alpha-iduronidase, iduronate-2 sulfatase, and aryl sulfatase.

13. A method for treating a subject with a central nervous system (CNS) disorder comprising administering to the subject:

a. a structure that binds to a receptor expressed on the blood brain barrier (BBB), wherein the structure comprises HIRMab; and

b. a glucose monosaccharide;

wherein the glucose monosaccharide and the structure are present in a same solution and wherein the administering treats the subject having the CNS disorder.

14. The method of claim 13 , wherein the solution comprises greater than 5% monosaccharide.

15. A method for treating a subject with a central nervous system (CNS) disorder, wherein the disorder is selected from the group consisting of Hurler's Syndrome, Hunter's Syndrome, Type I mucopolysaccharidosis, Type II mucopolysaccharidosis, and a lysosomal storage disorder, the method comprising administering to the subject:

a. a structure that binds to a receptor expressed on the blood brain barrier (BBB), wherein the structure comprises HIRMab; wherein the structure is a fusion antibody comprising: an amino acid sequence of a heavy chain immunoglobulin covalently linked to an amino acid sequence of a polypeptide which polypeptide comprises a lysosomal enzyme or an amino acid sequence of a light chain immunoglobulin covalently linked to an amino acid sequence of a polypeptide which polypeptide comprises a lysosomal enzyme; and wherein the lysosomal enzyme is selected from the group consisting of: alpha-iduronidase, iduronate-2 sulfatase, and aryl sulfatase; and

b. a glucose monosaccharide;

wherein the glucose monosaccharide and the structure are present in a same solution,

wherein the solution comprises greater than 5% monosaccharide, and wherein the administering treats the subject having the CNS disorder.

Assignments (2)
CONFIRMATORY LICENSE Recorded Feb 12, 2018
From: UNIVERSITY OF CALIFORNIA LOS ANGELES
To: NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT
Reel/Frame 045310/0263 →
CONFIRMATORY LICENSE Recorded Jun 23, 2016
From: UNIVERSITY OF CALIFORNIA LOS ANGELES
To: NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT
Reel/Frame 039128/0180 →
Continuity (3)
Provisional Application 61856499 · Jul 19, 2013
Provisional Application 61857186 · Jul 22, 2013
Related Publication 20160152719A1 · Jun 2, 2016