IP Library › Granted Patent US 9,795,627
Granted Patent B2
US 9,795,627 · App. 15/264,709 · Granted Oct 24, 2017

Method for prevention of colectomy

Inventors: Charlotte Admyre (Vendelsö, SE); Arezou Zargari (Solna, SE); Oliver Von Stein (Upplands Väsby, SE); Petra Von Stein (Upplands Väsby, SE)
Assignee: INDEX PHARMACEUTICALS AB
A61K31/713A61K39/0005A61K45/06C12N15/117C12N2310/17C12N2310/315C12N2320/31
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Quick Facts
Patent No.
US 9,795,627
App. No.
15/264,709
Granted
Oct 24, 2017
Kind
B2
Abstract

A method of treating chronic active ulcerative colitis in a subject that is refractory or responds insufficiently or is intolerant to anti-inflammatory therapy, comprises administering to a patient in need thereof an effective exposure of an oligonucleotide comprising the sequence 5′-GGAACAGTTCGTCCATGGC-3′ (SEQ ID NO.2), wherein at least one CG dinucleotide is unmethylated. The oligonucleotide is not administered with corticosteroids or glucocorticosteroids.

Claims (18)

1. A method of treating chronic active ulcerative colitis in a subject that is refractory or responds insufficiently or is intolerant to anti-inflammatory therapy, comprising administering to the subject an effective exposure of an oligonucleotide comprising the sequence 5′-GGAACAGTTCGTCCATGGC-3′ (SEQ ID NO:2), wherein at least one CG dinucleotide is unmethylated, and wherein said oligonucleotide is not administered in combination with corticosteroid or glucocorticosteroid.

2. The method of claim 1 , wherein at least one nucleotide in said oligonucleotide has a backbone modification.

3. The method of claim 2 , wherein said backbone modification is a phosphate backbone modification represented by a phosphorothioate or a phosphorodithioate modification.

4. The method of claim 2 , wherein said backbone modification is located in the 5′- and/or the 3′-end of said oligonucleotide.

5. The method of claim 1 , wherein said oligonucleotide has the sequence 5′-G*G*A*ACAGTTCGTCCAT*G*G*C-3′ (SEQ ID NO:1), wherein the CG dinucleotide is unmethylated.

6. The method of claim 1 , wherein individual doses of said oligonucleotide are repetitively administered as a single exposure.

7. The method of claim 1 , wherein two or more doses of said oligonucleotide are administered on two or more separate occasions 4 to 70 weeks apart.

8. The method of claim 1 , wherein the amount of said oligonucleotide administered is in the range from about 0.3 mg to about 100 mg.

9. The method of claim 1 , wherein the amount of said oligonucleotide administered is in the range from about 25 mg to about 60 mg.

10. The method of claim 1 , wherein the amount of said oligonucleotide administered is about 30 mg.

11. The method of claim 1 , wherein said oligonucleotide is administered in combination with one or more other drugs.

12. The method of claim 1 , wherein said oligonucleotide is administered in combination with one or more immunomodulatory drugs or anti-TNF therapy drugs.

13. The method of claim 1 , wherein said oligonucleotide is administered in combination with one or more of cylclosporine, Infliximab, Adallilumab, natural IFN-β, S-Ompeprazol, 5-Asa, or Azathioprin.

14. The method of claim 1 , wherein said oligonucleotide is administered topically to mucousal membranes.

15. The method of claim 1 , wherein said oligonucleotide is administered intracolonically.

16. The method of claim 1 , wherein said subject is elective for colectomy.

17. The method of claim 1 , wherein the oligonucleotide is administered in the form of a pharmaceutical composition comprising the oligonucleotide together with one or more pharmaceutically acceptable excipient(s) and/or carrier(s).

18. The method of claim 17 , wherein said composition comprises said oligonucleotide and water.

Priority Claims (1)
EP 11190826 · Nov 25, 2011 · regional
Continuity (3)
Continuation 14359945
Provisional Application 61595230 · Feb 6, 2012
Related Publication 20170014442A1 · Jan 19, 2017