IP Library Granted Patent US 10,772,939
Granted Patent B2
US 10,772,939 · App. 15/974,293 · Granted Sep 15, 2020

Fragments of P97 and uses thereof

Inventors: Timothy Z. Vitalis (Vancouver, CA); Reinhard Gabathuler (Montreal, CA)
Assignee: Bioasis Technologies, Inc.
A61K38/46A61K47/6849A61K47/6855A61K49/0002C07K7/06C07K7/08C07K14/79C07K16/00C07K16/32C12Y306/04006Y02A50/401Y02A50/473
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Quick Facts
Patent No.
US 10,772,939
App. No.
15/974,293
Granted
Sep 15, 2020
Kind
B2
Abstract

Provided are fragments of human p97 (melanotransferrin) polypeptides having blood-brain barrier (BBB) transport activity, including variants and combinations thereof, conjugates comprising the p97 fragments, and related methods of use thereof, for instance, to facilitate delivery of therapeutic or diagnostic agents across the BBB.

Claims (15)

1. A method for facilitating the transport of therapeutic agents across the blood brain barrier (BBB) comprising administering to a subject in need thereof, a pharmaceutical composition comprising a p97 fragment that is conjugated to a therapeutic agent optionally via a linker, to form a p97-agent conjugate, wherein the p97 fragment consists essentially of DSSHAFTLDELR (SEQ ID NO: 13).

2. The method of claim 1 , wherein the p97 fragment has one or more terminal cysteines and/or tyrosines.

3. The method of claim 2 wherein the p97 fragment consists of DSSHAFTLDELR (SEQ ID NO: 13) with a C-terminal tyrosine, and wherein the p97 fragment and the therapeutic agent are separated by a peptide linker of about 1-10 amino acids in length.

4. The method of claim 2 wherein the p97 fragment consists of DSSHAFTLDELR (SEQ ID NO: 13) with a C-terminal cysteine, and wherein the p97 fragment and the therapeutic agent are separated by a peptide linker of about 1-10 amino acids in length.

5. The method of claim 2 wherein the p97 fragment consists of DSSHAFTLDELR (SEQ ID NO: 13) with a N-terminal tyrosine, and wherein the p97 fragment and the therapeutic agent are separated by a peptide linker of about 1-10 amino acids in length.

6. The method of claim 2 wherein the p97 fragment consists of DSSHAFTLDELR (SEQ ID NO: 13) with a N-terminal cysteine, and wherein the p97 fragment and the therapeutic agent are separated by a peptide linker of about 1-10 amino acids in length.

7. The method of claim 1 , wherein the therapeutic agent of the conjugate is associated with a lysosomal storage disease.

8. The method of claim 1 , where the therapeutic agent is a molecule having a molecular weight of less than 2000 daltons, a polypeptide, a peptide mimetic, a peptoid, an aptamer, or a detectable entity.

9. The method of claim 7 , wherein the therapeutic agent is presented in a therapeutically effective amount to treat a lysosomal storage disease in a subject in need thereof.

10. The method of claim 9 wherein the therapeutically effective amount of the therapeutic agent is from about 0.001 mg/kg to about 100 mg/kg.

11. The method of claim 7 , where the lysosomal storage disease is selected from one or more of aspartylglucosaminuria, cholesterol ester storage disease, Wolman disease, cystinosis, Danon disease, Fabry disease, Farber lipogranulomatosis, Farber disease, fucosidosis, galactosialidosis types I/II, Gaucher disease types I/II/III, Gaucher disease, globoid cell leucodystrophy, Krabbe disease, glycogen storage disease II, Pompe disease, GM1-gangliosidosis types I/II/III, GM2-gangliosidosis type I, Tay Sachs disease, GM2-gangliosidosis type II, Sandhoff disease, GM2-gangliosidosis, α-mannosidosis types I/II, β-mannosidosis, metachromatic leucodystrophy, mucolipidosis type I, sialidosis types I/II mucolipidosis types II/III I-cell disease, mucolipidosis type IIIC pseudo-Hurler polydystrophy, mucopolysaccharidosis type I, mucopolysaccharidosis type II (Hunter syndrome), mucopolysaccharidosis type IIIA, Sanfilippo syndrome, mucopolysaccharidosis type IIIB, mucopolysaccharidosis type IIIC, mucopolysaccharidosis type IIID, mucopolysaccharidosis type IVA, Morquio syndrome, mucopolysaccharidosis type IVB, mucopolysaccharidosis type VI, mucopolysaccharidosis type VII, Sly syndrome, mucopolysaccharidosis type IX, multiple sulfatase deficiency, neuronal ceroid lipofuscinosis, CLN1 Batten disease, Niemann-Pick disease types NB, Niemann-Pick disease, Niemann-Pick disease type C1, Niemann-Pick disease type C2, pycnodysostosis, Schindler disease types I/II, Schindler disease, and sialic acid storage disease.

12. The method of claim 11 where the selected lysosomal storage disease is Fabry disease.

13. The method of claim 11 where the selected lysosomal storage disease is Gaucher disease.

14. The method of claim 11 where the selected lysosomal storage disease is mucopolysaccharidosis type I.

15. The method of claim 11 where the selected lysosomal storage disease is mucopolysaccharidosis type II (Hunter syndrome).

Assignments (2)
CORRECTIVE ASSIGNMENT TO CORRECT THE ADDRESS OF RECEIVING PARTY PREVIOUSLY RECORDED ON REEL 052466 FRAME 0894. ASSIGNOR(S) HEREBY CONFIRMS THE ASSIGNMENT. Recorded Aug 17, 2020
From: VITALIS, TIMOTHY Z.; GABATHULER, REINHARD
To: BIOASIS TECHNOLOGIES, INC.
Reel/Frame 053520/0336 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 22, 2020
From: VITALIS, TIMOTHY Z.; GABATHULER, REINHARD
To: BIOASIS TECHNOLOGIES, INC.
Reel/Frame 052466/0894 →
Continuity (5)
Continuation 15153074 · May 12, 2016
Continuation 14210029 · Mar 13, 2014
Provisional Application 61885387 · Oct 1, 2013
Provisional Application 61780170 · Mar 13, 2013
Related Publication 20190008929A1 · Jan 10, 2019