IP Library › Granted Patent US 11,939,361
Granted Patent B2
US 11,939,361 · App. 17/531,538 · Granted Mar 26, 2024

Compositions of peptide inhibitors of Interleukin-23 receptor

Inventors: Giustino Di Pretoro (Beerse, BE); Dajun Sun (Beerse, BE); Gopal Rajan (Beerse, BE); Geraldine Broeckx (Beerse, BE); Nathalie Mertens (Beerse, BE); Shu Li (Newark, CA); Felix Lai (Newark, CA); Mohammad Masjedizadeh (Newark, CA); Anne M. Fourie (San Diego, CA); Beverly Knight (San Diego, CA); David Polidori (Rancho Santa Fe, CA); Santhosh Francis Neelamkavil (Edison, NJ); Nishit Modi (Newark, CA); Ashok Bhandari (Pleasanton, CA); Xiaoli Cheng (Mountain View, CA)
Assignees: Janssen Pharmaceutica NV; Protagonist Therapeutics, Inc.
C07K14/4703A61K47/26A61K47/38A61K47/6923A61P37/00A61K38/00
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Quick Facts
Patent No.
US 11,939,361
App. No.
17/531,538
Granted
Mar 26, 2024
Kind
B2
Abstract

The present invention relates to compositions of peptide inhibitors of the interleukin-23 receptor (IL-23R) or pharmaceutically acceptable salt or solvate forms thereof, corresponding pharmaceutical compositions, methods and/or uses for treatment of autoimmune inflammation and related diseases and disorders.

Claims (25)

1. A pharmaceutical composition comprising:

a peptide of SEQ ID NO: 1 or a pharmaceutically acceptable salt or solvate form thereof in an amount of from about 0.1% to about 15% (w/w) of the pharmaceutical composition; and

one or more pharmaceutically acceptable excipients.

2. The pharmaceutical composition of claim 1 , wherein the peptide of SEQ ID NO: 1 or a pharmaceutically acceptable salt or solvate form thereof, has the chemical structure:

and wherein the peptide of SEQ ID NO: 1 or a pharmaceutically acceptable salt or solvate form thereof is a pharmaceutically acceptable salt form.

3. The pharmaceutical composition of claim 1 , wherein the peptide of SEQ ID NO: 1 or a pharmaceutically acceptable salt or solvate form thereof is an acetate form.

4. The pharmaceutical composition of claim 3 , wherein the acetate form is in an amorphous form.

5. The pharmaceutical composition of claim 1 , wherein the amount of the peptide of SEQ ID NO: 1 or a pharmaceutically acceptable salt or solvate form thereof is from about 1 mg to about 1000 mg.

6. The pharmaceutical composition of claim 1 , wherein the amount of the peptide of SEQ ID NO: 1 or a pharmaceutically acceptable salt or solvate form thereof is from about 10 mg to about 300 mg.

7. The pharmaceutical composition of claim 1 , wherein the amount of the peptide of SEQ ID NO: 1 or a pharmaceutically acceptable salt or solvate form thereof is from about 25 mg to about 150 mg.

8. The pharmaceutical composition of claim 1 , wherein the pharmaceutical composition further comprises an absorption enhancer.

9. The pharmaceutical composition of claim 8 comprising:

a peptide of SEQ ID NO: 1 or a pharmaceutically acceptable salt or solvate form thereof in an amount of from about 0.1% to about 15% (w/w) of the pharmaceutical composition;

an absorption enhancer in an amount from about 10% to about 60% (w/w); and

one or more pharmaceutically acceptable excipients.

10. A method of treating an inflammatory disease in a subject comprising administering to the subject a therapeutically effective amount of a pharmaceutical composition of claim 1 .

11. A pharmaceutical composition comprising:

a peptide of SEQ ID NO: 1 or a pharmaceutically acceptable salt or solvate form thereof in an amount of from about 0.1% to about 20% (w/w) of the pharmaceutical composition; and

one or more pharmaceutically acceptable excipients.

12. The pharmaceutical composition of claim 11 , wherein the peptide of SEQ ID NO: 1 or a pharmaceutically acceptable salt or solvate form thereof, has the chemical structure:

and wherein the peptide of SEQ ID NO: 1 or a pharmaceutically acceptable salt or solvate form thereof is a pharmaceutically acceptable salt form.

13. The pharmaceutical composition of claim 12 , wherein the amount of the peptide of SEQ ID NO: 1 or a pharmaceutically acceptable salt or solvate form thereof is from about 1 mg to about 1000 mg.

14. The pharmaceutical composition of claim 13 , wherein the amount of the peptide of SEQ ID NO: 1 or a pharmaceutically acceptable salt or solvate form thereof is from about 10 mg to about 500 mg.

15. The pharmaceutical composition of claim 14 , wherein the amount of the peptide of SEQ ID NO: 1 or a pharmaceutically acceptable salt or solvate form thereof is from about 10 mg to about 300 mg.

16. A method of treating an inflammatory disease in a subject comprising administering to the subject a therapeutically effective amount of a pharmaceutical composition of claim 11 .

Assignments (6)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 26, 2023
From: BHANDARI, ASHOK; CHENG, XIAOLI
To: PROTAGONIST THERAPEUTICS, INC.
Reel/Frame 063452/0629 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 12, 2023
From: FOURIE, ANNE M.; KNIGHT, BEVERLY; NEELAMKAVIL, SANTHOSH FRANCIS; POLIDORI, DAVID
To: JANSSEN RESEARCH & DEVELOPMENT, LLC
Reel/Frame 063301/0029 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 12, 2023
From: JANSSEN RESEARCH & DEVELOPMENT, LLC
To: JANSSEN PHARMACEUTICA NV
Reel/Frame 063301/0132 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 12, 2023
From: MODI, NISHIT
To: PROTAGONIST THERAPEUTICS, INC.
Reel/Frame 063303/0134 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 8, 2022
From: DI PRETORO, GIUSTINO; SUN, DAJUN; RAJAN, GOPAL; BROECKX, GERALDINE; MERTENS, NATHALIE
To: JANSSEN PHARMACEUTICA NV
Reel/Frame 059200/0280 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 8, 2022
From: LI, SHU; LAI, FELIX; MASJEDIZADEH, MOHAMMAD
To: PROTAGONIST THERAPEUTICS, INC.
Reel/Frame 059200/0482 →
Continuity (3)
Provisional Application 63275222 · Nov 3, 2021
Provisional Application 63116568 · Nov 20, 2020
Related Publication 20220177532A1 · Jun 9, 2022