IP Library Granted Patent US 9,301,955
Granted Patent B2
US 9,301,955 · App. 14/397,743 · Granted Apr 5, 2016

Tritoqualine for use in the treatment of cystic fibrosis

Inventor: Dominique Costantini (Paris, FR)
Assignee: ORPHAN SYNERGY EUROPE-PHARMA
A61K31/4741
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Quick Facts
Patent No.
US 9,301,955
App. No.
14/397,743
Granted
Apr 5, 2016
Kind
B2
Abstract

This invention relates to tritoqualine for use in the treatment of cystic fibrosis or any one of its complications. The invention also relates to the method for the treatment of cystic fibrosis or any one of its complications by administering tritoqualine. The invention can be used to improve the condition of individuals with cystic fibrosis.

Claims (14)

1. A method for the treatment of cystic fibrosis in a subject in need of such treatment, wherein said method comprises administering to said subject an effective amount of tritoqualine.

2. The method according to claim 1 , wherein tritoqualine is administered to the subject in need of such treatment at a dose of 1 mg-4 g/day.

3. The method according to claim 1 , wherein tritoqualine is administered to the subject in need of such treatment at a dose of 1, 5, 10, 20, 30, 50, 100, 200, 300, 400, 500, or 600 mg/day.

4. The method according to claim 1 , wherein tritoqualine is administered to the subject in need of such treatment at a dose of 1 g/day, 2 g/day, 3 g/day or 4 g/day.

5. A method for the treatment of any complication of cystic fibrosis in a subject with cystic fibrosis, wherein said method comprises administering to said subject an effective amount of tritoqualine.

6. The method according to claim 5 , wherein the cystic fibrosis complications are selected from infection or inflammatory disorders.

7. The method according to claim 5 , wherein the cystic fibrosis complications are selected from infection or inflammatory disorders in the respiratory tract, pancreas, gastrointestinal tract, sweat glands, or other exocrine tissues.

8. The method according to claim 5 , wherein the cystic fibrosis complications are selected in the group consisting of severe chronic lung disease, pancreatic insufficiency, nasal polyposis, pansinusitis, chronic diarrhea, pancreatitis, cirrhosis or other forms of hepatic dysfunction, sinus disease, diabetes, and hepatobiliary problems.

9. The method according to claim 5 , wherein the treatment is the treatment of any of airway or nasal complications associated with cystic fibrosis.

10. The method according to claim 5 , wherein the treatment is a treatment of any of airway or nasal complications associated with cystic fibrosis and wherein the airway or nasal complications associated with cystic fibrosis is selected from the group consisting of lung disease, nasal polyposis, pansinusitis, and sinus disease.

11. The method according to claim 5 , wherein the cystic fibrosis complications are selected from the group consisting of focal biliary cirrhosis, biliary obstruction and progressive periportal fibrosis.

12. The method according to claim 5 , wherein tritoqualine is administered to the subject in need of such treatment at a dose of 1 mg-4 g/day.

13. The method according to claim 5 , wherein tritoqualine is administered to the subject in need of such treatment at a dose of 1, 5, 10, 20, 30, 50, 100, 200, 300, 400, 500, or 600 mg/day.

14. The method according to claim 5 , wherein tritoqualine is administered to the subject in need of such treatment at a dose of 1 g/day, 2 g/day, 3 g/day or 4 g/day.

Assignments (2)
CHANGE OF NAME Recorded Jan 18, 2018
From: ORPHAN SYNERGY EUROPE-PHARMA
To: OSE IMMUNOTHERAPEUTICS
Reel/Frame 045084/0702 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 12, 2015
From: COSTANTINI, DOMINIQUE
To: ORPHAN SYNERGY EUROPE - PHARMA
Reel/Frame 034679/0935 →
Priority Claims (1)
EP 12305487 · Apr 30, 2012 · regional
Continuity (1)
Related Publication 20150133487A1 · May 14, 2015