IP Library Granted Patent US 11,452,728
Granted Patent B2
US 11,452,728 · App. 15/661,586 · Granted Sep 27, 2022

7-aminocephalosporanic acid derivative as inhibitor of IL15 and IL-2 activity

Inventors: Katarzyna Koziak (Warsaw, PL); Barbara Zyzynska-Granica (Warsaw, PL); Slawomir Filipek (Warsaw, PL); Szymon Niewieczerzal (Warsaw, PL); Bartosz Trzaskowski (Warsaw, PL); Oliwia Zegrocka-Stendel (Lomianki, PL); Malgorzata Dutkiewicz (Warsaw, PL); Piotr Krzeczynski (Warsaw, PL); Elzbieta Kaczmarek (Warsaw, PL); Magdalena Winiarska (Warsaw, PL)
Assignee: Bio Research Project PSA
A61K31/546A61K9/0019
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Quick Facts
Patent No.
US 11,452,728
App. No.
15/661,586
Granted
Sep 27, 2022
Kind
B2
Abstract

The invention relates to a 7-aminocephalosporanic acid derivative, Cefazolin, for use as an inhibitor of IL-15 and IL-2 receptors in the prevention and treatment of diseases related to IL-15 and IL-2 overproduction.

Claims (29)

1. A method of treating psoriasis in a patient comprising:

(1) a step of identifying a patient having elevated levels of one or more selected from the group consisting of IL-2, IL-15, IL-17, and TNF-α; and

(2) a step of treating the patient by administering to the patient in need thereof a therapeutically effective dose Cefazolin or pharmaceutically acceptable salts thereof or pharmaceutically acceptable composition thereof wherein the pharmaceutically acceptable compositions comprise a therapeutically effective dose of Cefazolin or pharmaceutically acceptable salts thereof and a pharmaceutically acceptable excipient, carrier or diluent.

2. The method according to claim 1 , wherein the pharmaceutically acceptable compositions are administered intravenously or intramuscularly.

3. The method of claim 1 wherein the therapeutically effective dose of Cefazolin administered is sufficient to provide a serum concentration between 20 μm and 300 μm.

4. The method of claim 1 wherein the therapeutically effective dose of Cefazolin initially administered is between 250 and 500 mg followed by administration of a therapeutically effective dose between 250 and 500 mg of Cefazolin after an interval of between 8 to 12 hours.

5. The method of claim 1 , wherein the method comprises either:

i) administering to the patient in need thereof the therapeutically effective dose of Cefazolin or pharmaceutically acceptable salts thereof, wherein the Cefazolin or pharmaceutically acceptable salts thereof is the sole active ingredient, or

ii) administering to the patient in need thereof the pharmaceutically acceptable composition, wherein the Cefazolin or pharmaceutically acceptable salts thereof is the sole active ingredient.

6. A method of reducing the amount of IL-15 and/or IL-2 in a patient having psoriasis comprising:

(1) a step of identifying a patient having elevated levels of one or more selected from the group consisting of IL-2 and IL-15: and

(2) a step of treating the patient by administering to the patient in need thereof a therapeutically effective dose of Cefazolin or pharmaceutically acceptable salts thereof or pharmaceutically acceptable compositions thereof wherein the pharmaceutically acceptable compositions comprise a therapeutically effective dose of Cefazolin or pharmaceutically acceptable salts thereof and a pharmaceutically acceptable excipient, carrier or diluent.

7. The method of claim 6 wherein the therapeutically effective dose of Cefazolin is administered intravenously or intramuscularly.

8. The method of claim 6 wherein the therapeutically effective dose of Cefazolin administered is sufficient to provide a serum concentration between 20 μM and 300 μM.

9. The method of claim 6 , wherein the method comprises either:

i) administering to the patient in need thereof the therapeutically effective dose of Cefazolin or pharmaceutically acceptable salts thereof, wherein the Cefazolin or pharmaceutically acceptable salts thereof is the sole active ingredient, or

ii) administering to the patient in need thereof the pharmaceutically acceptable composition, wherein the Cefazolin or pharmaceutically acceptable salts thereof is the sole active ingredient.

10. A method for reducing synthesis of TNF-α and/or IL-17 in a patient having psoriasis comprising:

(1) a step of identifying a patient having elevated levels of one or more selected from the group consisting of IL-17 and TNF-α; and

(2) a step of treating the patient by parenterally administering to the patient in need thereof a therapeutically effective dose of Cefazolin or pharmaceutically acceptable salts thereof or pharmaceutically acceptable compositions thereof wherein the pharmaceutically acceptable compositions comprise a therapeutically effective dose of Cefazolin or pharmaceutically acceptable salts thereof and a pharmaceutically acceptable excipient, carrier or diluent.

11. The method of claim 10 , wherein the method comprises either:

i) administering to the patient in need thereof the therapeutically effective dose of Cefazolin or pharmaceutically acceptable salts thereof, wherein the Cefazolin or pharmaceutically acceptable salts thereof is the sole active ingredient, or

ii) administering to the patient in need thereof the pharmaceutically acceptable composition, wherein the Cefazolin or pharmaceutically acceptable salts thereof is the sole active ingredient.

12. A method for preventing overproduction of IL-15 and/or IL-2 in a patient having psoriasis comprising:

(1) a step of identifying a patient having psoriasis associated with overproduction of one or more selected from the group consisting of IL-2 and IL-15; and

(2) a step of treating the patient by administering to the patient in need thereof a therapeutically effective dose of Cefazolin or pharmaceutically acceptable salts thereof or pharmaceutically acceptable compositions thereof wherein the pharmaceutically acceptable compositions comprise a therapeutically effective dose of Cefazolin or pharmaceutically acceptable salts thereof and a pharmaceutically acceptable excipient, carrier or diluent.

13. The method of claim 12 , wherein the method comprises either:

i) administering to the patient in need thereof the therapeutically effective dose of Cefazolin or pharmaceutically acceptable salts thereof, wherein the Cefazolin or pharmaceutically acceptable salts thereof is the sole active ingredient, or

ii) administering to the patient in need thereof the pharmaceutically acceptable composition, wherein the Cefazolin or pharmaceutically acceptable salts thereof is the sole active ingredient.

Assignments (4)
CHANGE OF NAME Recorded Jul 3, 2024
From: BIO RESEARCH PROJECT PSA
To: BIORESEARCH PHARMA S.A.
Reel/Frame 068122/0063 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 14, 2022
From: KATARZYNA KOZIAK
To: BIO RESEARCH PROJECT PSA
Reel/Frame 058656/0456 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 14, 2022
From: WARSZAWSKI UNIWERSYTET MEDYCZNY
To: KATARZYNA KOZIAK
Reel/Frame 058773/0807 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Oct 12, 2017
From: KOZIAK, KATARZYNA; ZYZYNSKA-GRANICA, BARBARA; FILIPEK, SLAWOMIR; NIEWIECZERZAL, SZYMON; TRZASKOWSKI, BARTOSZ; ZEGROCKA-STENDEL, OLIWIA; DUTKIEWICZ, MALGORZATA; KRZECZYNSKI, PIOTR; KACZMAREK, ELZBIETA; WINIARSKA, MAGDALENA
To: WARSZAWSKI UNIWERSYTET MEDYCZNY
Reel/Frame 043847/0091 →
Priority Claims (1)
PL 405506 · Sep 30, 2013 · national
Continuity (2)
Division 15026125
Related Publication 20170319593A1 · Nov 9, 2017