IP Library Granted Patent US 10,874,714
Granted Patent B2
US 10,874,714 · App. 14/954,696 · Granted Dec 29, 2020

Method of treating fibroblast growth factor 21 (FGF-21) deficiency

Inventor: Shawn DeFrees (North Wales, PA)
Assignee: 89BIO LTD.
A61K38/1825A61K47/549A61K47/60C07K14/50C12P21/005A61K38/00
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Quick Facts
Patent No.
US 10,874,714
App. No.
14/954,696
Granted
Dec 29, 2020
Kind
B2
Abstract

The present invention relates to mutants of Fibroblast Growth Factor (FGF), particularly FGF-20 and FGF-21, which contain newly introduced N-linked or O-linked glycosylation site(s). The polynucleotide coding sequences for the mutants, expression cassettes comprising the coding sequences, cells expressing the mutants, and methods for producing the mutants are also disclosed. Further disclosed are pharmaceutical compositions comprising the mutants and method for using the mutants.

Claims (20)

1. A method of treating FGF-21 deficiency in a patient, comprising administering an effective amount of a Fibroblast Growth Factor-21 (FGF-21) conjugate to the patient, wherein the FGF-21 conjugate comprises a mutant FGF-21 peptide and a modifying group, wherein the mutant FGF-21 peptide comprises SEQ ID NO: 146 except for the presence of at least one O-linked or N-linked glycosylation site not present in SEQ ID NO: 146, wherein the mutant FGF-21 peptide comprises at least one amino acid sequence selected from the group consisting of SEQ ID NOs: 161-187, 189-214, 220-250, 252-271, 273-318, and 327-360, wherein the O-linked glycosylation site is a serine or threonine residue and the N-linked glycosylation site is an asparagine, and wherein the O-linked or N-linked glycosylation site is present at a site within one or more of SEQ ID NOs: 161-187, 189-214, 220-250, 252-271, 273-318, and 327-360, wherein said modifying group is covalently attached to said peptide at a preselected glycosyl or amino acid residue of said peptide via an intact glycosyl linking group, wherein said modifying group is not a naturally occurring saccharide moiety, and wherein the FGF-21 conjugate retains a biological activity of SEQ ID NO: 146, thereby treating the FGF-21 deficiency in the patient.

2. The method of claim 1 , wherein said FGF-21 peptide is at least 95% homologous to the amino acid sequence of SEQ I) NO 146.

3. The method of claim 1 , wherein said modifying group is covalently attached at said preselected glycosyl residue.

4. The method of claim 3 , wherein said modifying group is a non-glycosidic modifying group.

5. The method of claim 4 , wherein said non-glycosidic modifying group is a linear PEG or a branched PEG.

6. The method of claim 1 , wherein said glycosyl linking group has a structure according to the following formula:

wherein

R 2 is H, CH 2 OR 7 , COOR 7 or OR 7 , wherein R 7 represents H, substituted or unsubstituted alkyl, or substituted or unsubstituted heteroalkyl;

R 3 and R 4 are members independently selected from the group consisting of H, substituted or unsubstituted alkyl, OR 8 , and NHC(O)R 9 , wherein R 8 and R 9 are independently selected from the group consisting of H, substituted or unsubstituted alkyl, substituted or unsubstituted heteroalkyl, and sialic acid;

L a is a linker selected from the group consisting of a bond, substituted or unsubstituted alkyl, and substituted or unsubstituted heteroalkyl;

R 16 and R 17 are independently selected polymeric arms;

X 2 and X 4 are independently selected linkage fragments joining polymeric moieties R 16 and R 17 to C; and

X 5 is a non-reactive group.

7. The method of claim 1 , wherein said glycosyl linking group has a structure according to the following formula:

wherein

R 2 is H, CH 2 OR 7 , COOR 7 or OR 7 , wherein R 7 represents H, substituted or unsubstituted alkyl, or substituted or unsubstituted heteroalkyl;

R 3 and R 4 are members independently selected from the group consisting of H, substituted or unsubstituted alkyl, OR 8 , and NHC(O)R 9 , wherein R 8 and R 9 are independently selected from the group consisting of H, substituted or unsubstituted alkyl, substituted or unsubstituted heteroalkyl, and sialic acid;

R 16 and R 17 are independently selected polymeric arms; and

X 4 is a linkage fragment joining polymeric moiety R 17 to C.

8. The method of claim 1 , wherein said modifying group is selected from the group consisting of water-soluble polymers, therapeutic moieties, diagnostic moieties, targeting moieties, and biomolecules.

Assignments (7)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Oct 6, 2025
From: 89BIO LTD.
To: 89BIO, INC.
Reel/Frame 072478/0305 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 14, 2023
From: DEFREES, SHAWN
To: NEOSE TECHNOLOGIES, INC
Reel/Frame 062981/0931 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 14, 2023
From: NEOSE TECHNOLOGIES, INC
To: NOVO NORDISK A/S
Reel/Frame 062981/0963 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 8, 2020
From: NOVO NORDISK A/S
To: RATIOPHARM GMBH
Reel/Frame 053147/0057 →
CORRECTIVE ASSIGNMENT TO CORRECT THE APPLICATION NUMBER 62/623342 PREVIOUSLY RECORDED ON REEL 050112 FRAME 0408. ASSIGNOR(S) HEREBY CONFIRMS THE LICENSE ASSIGNMENT. Recorded Oct 24, 2019
From: RATIOPHARM GMBH; TEVA BRANDED PHARMACEUTICAL PRODUCTS R&D, INC.; TEVA PHARMACEUTICAL INDUSTRIES LTD.
To: 89BIO LTD.
Reel/Frame 050817/0001 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Aug 21, 2019
From: RATIOPHARM GMBH; TEVA BRANDED PHARMACEUTICAL PRODUCTS R&D, INC.; TEVA PHARMACEUTICAL INDUSTRIES LTD.
To: 89BIO LTD.
Reel/Frame 050112/0408 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Feb 13, 2019
From: RATIOPHARM GMBH
To: 89BIO LTD.
Reel/Frame 048318/0006 →
Continuity (4)
Division 13332708 · Dec 21, 2011
Division 11665908
Provisional Application 60623342 · Oct 29, 2004
Related Publication 20160158319A1 · Jun 9, 2016