IP Library Granted Patent US 10,537,543
Granted Patent B2
US 10,537,543 · App. 16/279,819 · Granted Jan 21, 2020

Pharmaceutical compositions comprising DGLA and use of same

Inventors: Mehar Manku (Birmingham, GB); John Climax (Dublin, IE); David Coughlan (Dublin, IE); James Dunne (Dublin, IE)
Assignee: DS Biopharma Limited
A61K31/202A61P17/04A61K9/0053
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Quick Facts
Patent No.
US 10,537,543
App. No.
16/279,819
Granted
Jan 21, 2020
Kind
B2
Abstract

The present disclosure provides orally deliverable pharmaceutical compositions comprising DGLA and to methods of using same to treat a variety of conditions and disorders.

Claims (14)

1. A method for administering dihomo gamma linolenic acid (DGLA) to a human patient, the method comprising orally administering an effective dose of DGLA to a human patient having a skin disease under fasting conditions that are effective to treat the skin disease.

2. The method of claim 1 , wherein the effective dose of DGLA is at least about 500 mg per day.

3. The method of claim 1 , wherein the skin disease is atopic dermatitis or pruritus.

4. The method of claim 3 , wherein the atopic dermatitis is mild atopic dermatitis, moderate atopic dermatitis, or severe atopic dermatitis.

5. The method of claim 1 , wherein the DGLA is in a form of a triglyceride, an alkyl ester, a free fatty acid, or a salt.

6. The method of claim 1 , wherein the effective dose is administered to the subject daily for a period of at least about 8 weeks.

7. The method of claim 1 wherein the effective dose of DGLA is 500 mg-2000 mg per day.

8. A method of treating a skin disease in a fasting subject, the method comprising orally administering an effective dose of a pharmaceutical comprising at least 95% DGLA, by weight of total fatty acids, to a fasting subject having a skin disease.

9. The method of claim 8 , wherein the fasting conditions further comprise no food prior to administration of the effective dose of DGLA and no liquids, besides water, prior to administration of the effective dose of DGLA.

10. The method of claim 9 , wherein the effective dose of DGLA is at least 500 mg per day.

11. The method of claim 10 , wherein the skin disease is atopic dermatitis or pruritus, and wherein the atopic dermatitis is mild atopic dermatitis, moderate atopic dermatitis, or severe atopic dermatitis.

12. The method of claim 11 , wherein the DGLA is in a form of a triglyceride, an alkyl ester, a free fatty acid, or a salt.

13. The method of claim 11 , wherein the effective dose is administered to the subject daily for a period of at least about 8 weeks.

14. The method of claim 8 wherein the effective dose of DGLA is 500 mg-2000 mg per day.

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 24, 2019
From: MANKU, MEHAR; CLIMAX, JOHN; COUGHLAN, DAVID; DUNNE, JAMES
To: DIGNITY SCIENCES LIMITED
Reel/Frame 049850/0053 →
CHANGE OF NAME Recorded Jul 24, 2019
From: DIGNITY SCIENCES LIMITED
To: DS BIOPHARMA LIMITED
Reel/Frame 049850/0253 →
Continuity (8)
Continuation 15935739 · Mar 26, 2018
Continuation 15842194 · Dec 14, 2017
Continuation 15661374 · Jul 27, 2017
Continuation 15343689 · Nov 4, 2016
Continuation 14730818 · Jun 4, 2015
Provisional Application 62058469 · Oct 1, 2014
Provisional Application 62007752 · Jun 4, 2014
Related Publication 20190274989A1 · Sep 12, 2019