IP Library Patent Application 13857295
Patent Application
App. No. 13/857,295

METHOD FOR TREATING INTESTINAL DISEASES PRESENTING AT LEAST ONE INFLAMMATORY COMPONENT

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Patent No.
US None
App. No.
13/857,295
Abstract

The present disclosure relates to methods for treating intestinal diseases presenting at least one inflammatory component such as inflammatory bowel disease or diverticular disease and/or maintaining remission of intestinal diseases presenting at least one inflammatory component such as inflammatory bowel disease (IBD) or diverticular disease using budesonide MMX compositions.

Claims (29)

1 . A method of treating ulcerative colitis in a patient in need of such treatment, said patient having been previously administered a composition comprising 5-aminosalicylic acid, said method comprising administering to said patient a second composition in the form of a single tablet, said single tablet comprising about 9 mg of budesonide.

2 . A method according to claim 1 , wherein said second composition is administered to said patient for up to 8 weeks or a portion thereof.

3 . A method according to claim 1 , wherein said patient has a UCDAI score of greater than or equal to 4 prior to said second composition being administered to said patient.

4 . A method according to claim 3 , wherein second composition is administered to said patient once daily for up to 8 weeks or a portion thereof.

5 . A method according to claim 4 , wherein after said treatment, said UCDAI score for said patient is less than or equal to 1.

6 . A method according to claim 1 , wherein said patient is experiencing an ulcerative colitis flare prior to said second composition being administered to said patient.

7 . A method according to claim 6 , wherein said second composition is administered to said patient once daily for up to 8 weeks or a portion thereof.

8 . A method according to claim 7 , wherein said ulcerative colitis in said patient is in remission after said treatment.

9 . A method of treating ulcerative colitis in a patient in need of such treatment, said method comprising administering to said patient a first and a second composition, said first composition comprising 5-aminosalicylic acid and said second composition is in the form of a single tablet, said single tablet comprising about 9 mg of budesonide.

10 . A method according to claim 9 , wherein said second composition is administered to said patient for up to 8 weeks or a portion thereof.

11 . A method according to claim 9 , wherein said patient has a UCDAI score of greater than or equal to 4 prior to said second composition being administered to said patient.

12 . A method according to claim 11 , wherein said second composition is administered to said patient once daily for up to 8 weeks or a portion thereof.

13 . A method according to claim 12 , wherein after said treatment, said UCDAI score for said patient is less than or equal to 1.

14 . A method according to claim 9 , wherein said patient is experiencing an ulcerative colitis flare prior to said second composition being administered to said patient.

15 . A method according to claim 14 , wherein second composition is administered to said patient once daily for up to 8 weeks or a portion thereof.

16 . A method according to claim 15 , wherein said ulcerative colitis in said patient is in remission after said treatment.

17 . A method according to claim 9 , wherein said first composition and said second composition are administered to said patient simultaneously.

18 . A method of treating ulcerative colitis in a patient in need of such treatment, said patient having been previously administered a composition comprising 5-aminosalicylic acid, said method comprising administering to said patient a first composition and a second composition, said first composition comprising 5-aminosalicylic acid and said second composition is in the form of a single tablet, said single tablet comprising about 9 mg of budesonide.

19 . A method according to claim 18 , wherein second composition is administered to said patient for up to 8 weeks or a portion thereof.

20 . A method according to claim 19 , wherein said patient has a UCDAI score of greater than or equal to 4 prior to said second composition being administered to said patient.

21 . A method according to claim 20 , wherein second composition is administered to said patient once daily for up to 8 weeks or a portion thereof.

22 . A method according to claim 21 , wherein after said treatment, said UCDAI score for said patient is less than or equal to 1.

23 . A method according to claim 18 , wherein said patient is experiencing an ulcerative colitis flare prior to said second composition being administered to said patient.

24 . A method according to claim 23 , wherein second composition is administered to said patient once daily for up to 8 weeks or a portion thereof.

25 . A method according to claim 24 , wherein said ulcerative colitis in said patient is in remission after said treatment.

26 . A method according to claim 18 , wherein said first composition and said second composition are administered to said patient simultaneously.

27 . A method of maintaining remission of ulcerative colitis in a patient in need of such maintenance, said method comprising administering to said patient a composition in the form of a single tablet, said single tablet comprising about 6 mg of budesonide, whereby said remission of ulcerative colitis in said patient is maintained.

28 . A method according to claim 27 , wherein said single tablet comprising about 6 mg of budesonide is administered to said patient once daily for up to 12 months.

29 . A method according to claim 28 , wherein said single tablet comprising about 6 mg of budesonide is administered to said patient once daily for up to 6 months.

Assignments (4)
RELEASE OF SECURITY INTEREST Recorded Apr 8, 2025
From: BARCLAYS BANK PLC, AS COLLATERAL AGENT
To: SOLTA MEDICAL, INC.; PRECISION DERMATOLOGY, INC.; BAUSCH HEALTH IRELAND LIMITED (F/K/A/ VALEANT PHARMACEUTICALS IRELAND LIMITED); SALIX PHARMACEUTICALS, INC.; SALIX PHARMACEUTICALS, LTD; SANTARUS, INC.; MEDICIS PHARMACEUTICAL CORPORATION; HUMAX PHARMACEUTICAL S.A.; SOLTA MEDICAL IRELAND LIMITED; BAUSCH & LOMB MEXICO, S.A. DE C.V.; BAUSCH+LOMB OPS B.V.; BAUSCH HEALTH AMERICAS, INC.; BAUSCH HEALTH COMPANIES INC.; BAUSCH HEALTH HOLDCO LIMITED; BAUSCH HEALTH MAGYARORSZAG KFT (A/K/A BAUSCH HEALTH HUNGARY LLC); BAUSCH HEALTH POLAND SPOLKA Z OGRANICZONA ODPOWIEDZIALNOSCIA (F/K/A VALEANT PHARMA POLAND SPOLKA Z OGRANICZONA ODPOWIEDZIALNOSCIA); BAUSCH HEALTH US, LLC; BAUSCH HEALTH, CANADA INC. / SANTE BAUSCH, CANADA INC.; ICN POLFA RZESZOW SPOLKA AKCYJNA (A/K/A ICN POLFA RZESZOW S.A.); ORAPHARMA, INC.; PRZEDSIEBIORSTWO FARMACEUTYCZNE JELFA SPOLKA AKCYJNA (A/K/A PRZEDSIEBIORSTWO FARMACEUTYCZNE JELFA S.A.); SOLTA MEDICAL DUTCH HOLDINGS B.V.; V-BAC HOLDING CORP.; VRX HOLDCO LLC; 1261229 B.C. LTD.; 1530065 B.C. LTD.
Reel/Frame 070778/0199 →
SECURITY AGREEMENT Recorded Apr 2, 2015
From: GLYCYX PHARMACEUTICALS, LTD.; SALIX PHARMACEUTICALS, INC.; SALIX PHARMACEUTICALS, LTD.; SANTARUS, INC.
To: BARCLAYS BANK PLC, AS COLLATERAL AGENT
Reel/Frame 035364/0396 →
RELEASE OF SECURITY INTEREST Recorded Apr 1, 2015
From: JEFFERIES FINANCE LLC
To: SANTARUS, INC.
Reel/Frame 035353/0836 →
SECURITY AGREEMENT Recorded Jan 2, 2014
From: SANTARUS, INC.
To: JEFFERIES FINANCE LLC, AS COLLATERAL AGENT
Reel/Frame 031910/0545 →