(CB-01-02/04) Extension Study of Budesonide Multi-Matrix System (MMX) 6 mg in Maintenance Of Remission In Patients With Ulcerative Colitis.
- Conditions
- Ulcerative Colitis
- Interventions
- Drug: Placebo Tablet
- Registration Number
- NCT00801723
- Lead Sponsor
- Bausch Health Americas, Inc.
- Brief Summary
Randomized, double-blind, comparative study versus placebo performed in patients from studies CB-01-02/01 (NCT00679432), CB-01-02/02 (NCT00679380), or CB-01-02/06 (NCT01100112) who achieved ulcerative colitis disease activity index (UCDAI) remission after 8 weeks of treatment.
Patients in remission at the End of Study visit will be given the opportunity to enter the 12-month Maintenance Phase study outlined in this protocol (CB-01-02/04). The End of Study visit in studies 01, 02, and 06 will be set as the Visit 1 (Day 0) of this study. There will be no interruption of study treatment between the parent studies and this study.
It is planned that approximately 150 patients will be enrolled in the study. Patients will be randomly assigned to two groups to receive either budesonide MMX 6 mg or placebo irrespective of the treatment assigned in studies 01, 02, or 06. Treatments will be administered once a day after breakfast for a maximum of 12 months or up to the occurrence of the first clinical relapse, where clinical relapse is defined as combined recurrence of rectal bleeding and stool frequency ≥ 1-2 stools/day above normal for the patient (score ≥ 1 in both UCDAI items).
During the study, patients will be assessed for safety and efficacy at Visit 1 and after 1, 3, 6, 9, and 12 months of treatment.
Patients will be contacted by telephone on a monthly basis for safety assessment. In case of occurrence of symptoms suggestive of clinical relapse, patients will attend an unscheduled visit at any time during the study.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 123
-
Patients fulfilling the following criteria are eligible for participation in the study:
- Male and female patients, 18-75 years old, who are able to understand and voluntarily provide written informed consent.
- Patients in UCDAI remission defined as a UCDAI score ≤ 1 point with a score of 0 for rectal bleeding and stool frequency, and a ≥ 1 point reduction from baseline in the endoscopy score without any sign of mucosal friability (score 0 for mucosal appearance).
- Patients who have completed all End of Study assessments for the CB-01-02/01, CB-01-02/02 and CB-01-02/06 studies.
- Females of child-bearing potential must have had a serum pregnancy test performed at the End of Study visit of the parent studies and must use an acceptable contraceptive method throughout the study treatment period.
-
Patients who meet any of the following criteria at screening visit are to be excluded from study participation:
- Subjects who have withdrawn from studies CB-01-02/01, CB 01 02/02 or CB-01-02/06.
- Subjects who did not achieve induction of remission according to the primary endpoint definition in studies CB-01-02/01, CB 01 02/02 or CB-01-02/06 (i.e. clinical remission defined as a UCDAI score ≤ 1 point with a score of 0 for rectal bleeding and stool frequency, and ≥ 1 point reduction from baseline in the endoscopy score without any sign of mucosal friability [score 0 for mucosal appearance]).
- Subjects with bone density lower than normal by age and sex (T-score lower than -1) as assessed via dual energy X-ray absorptiometry (DXA) scans.
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description 1: Budesonide MMX® 6 mg Budesonide MMX 6 mg Tablet One Budesonide-MMX® 6 mg tablet self-administered by the patients with a glass of water, in the morning after breakfast. 2: Placebo Placebo Tablet One placebo tablet self-administered by the patients with a glass of water, in the morning after breakfast.
- Primary Outcome Measures
Name Time Method Percentage of Participants Achieving Clinical Remission 1, 3, 6, 9, and 12 months Clinical remission was defined as the combined absence of recurrence of rectal bleeding and absence of increased stool frequency.
- Secondary Outcome Measures
Name Time Method Percentage of Participants With Clinical Relapse 12 months Clinical relapse was defined as the recurrence of rectal bleeding and/or an abnormal stool frequency \[≥ 1-2 stools/day above normal for the participant. Clinical remission/relapse status was based on participant diary entries prior to each scheduled visit.
Percentage of Participants With Endoscopic Relapse 12 months Endoscopic relapse was defined as an increase of ≥ 2 points in the Endoscopic Index score from the value calculated at baseline. The score is comprised of four components (granulated scattering reflected light, vascular pattern, vulnerability of mucosa, and mucosal damage). Scores range from 0 to 12, and higher scores indicate more severe (worse) endoscopic findings.
Trial Locations
- Locations (58)
Santarus Clinical Investigational Site 5077
🇺🇸Prince Frederick, Maryland, United States
Santarus Clinical Investigational Site 5067
🇺🇸San Diego, California, United States
Santarus Clinical Investigational Site 5044
🇺🇸Anaheim, California, United States
Santarus Clinical Investigational Site 5041
🇺🇸Hollywood, Florida, United States
Santarus Clinical Investigational Site 5016
🇺🇸Atlanta, Georgia, United States
Santarus Clinical Investigational Site 5068
🇺🇸Evanston, Illinois, United States
Santarus Clinical Investigational Site 5025
🇺🇸Baltimore, Maryland, United States
Santarus Clinical Investigational Site 6008
🇨🇦Victoria, British Columbia, Canada
Santarus Clinical Investigational Site 5011
🇺🇸Great Neck, New York, United States
Santarus Clinical Investigational Site 5045
🇺🇸Cincinnati, Ohio, United States
Santarus Clinical Investigational Site 5035
🇺🇸Sayre, Pennsylvania, United States
Santarus Clinical Investigational Site 5019
🇺🇸Houston, Texas, United States
Santarus Clinical Investigational Site 5097
🇺🇸Christiansburg, Virginia, United States
Santarus Clinical Investigational Site 5036
🇺🇸Houston, Texas, United States
Santarus Clinical Investigational Site 6006
🇨🇦Toronto, Ontario, Canada
Santarus Clinical Investigational Site 6013
🇨🇦Longueuil, Quebec, Canada
Santarus Clinical Investigational Site 5070
🇺🇸Palm Springs, California, United States
Santarus Clinical Investigational Site 5006
🇺🇸Troy, Michigan, United States
Santarus Clinical Investigational Site 5058
🇺🇸Huntersville, North Carolina, United States
Santarus Clinical Investigational Site 5055
🇺🇸New Smyrna Beach, Florida, United States
Santarus Clinical Investigational Site 5010
🇺🇸Chesterfield, Michigan, United States
Santarus Clinical Investigational Site 5064
🇺🇸Lakewood, Colorado, United States
Santarus Clinical Investigational Site 5089
🇺🇸Boynton Beach, Florida, United States
Santarus Clinical Investigational Site 5020
🇺🇸Pittsford, New York, United States
Santarus Clinical Investigational Site 5054
🇺🇸La Porte, Texas, United States
Santarus Clinical Investigational Site 5101
🇺🇸New York, New York, United States
Santarus Clinical Investigational Site 5004
🇺🇸Wyoming, Michigan, United States
Santarus Clinical Investigational Site 5072
🇺🇸Kingwood, Texas, United States
Santarus Clinical Investigational Site 6004
🇨🇦Richmond Hill, Ontario, Canada
Santarus Clinical Investigational Site 5063
🇺🇸Irving, Texas, United States
Santarus Clinical Investigational Site 5030
🇺🇸Lewisville, Texas, United States
Santarus Clinical Investigational Site 5093
🇺🇸Plano, Texas, United States
Santarus Clinical Investigational Site 5076
🇺🇸Houston, Texas, United States
Santarus Clinical Investigational Site 5088
🇺🇸Tucson, Arizona, United States
Santarus Clinical Investigational Site 5051
🇺🇸Huntsville, Alabama, United States
Santarus Clinical Investigational Site 5087
🇺🇸Lakewood, California, United States
Santarus Clinical Investigational Site 5033
🇺🇸Los Angeles, California, United States
Santarus Clinical Investigational Site 5074
🇺🇸Port Orange, Florida, United States
Santarus Clinical Investigational Site 5047
🇺🇸Winter Park, Florida, United States
Santarus Clinical Investigational Site 5056
🇺🇸Columbus, Georgia, United States
Santarus Clinical Investigational Site 5003
🇺🇸Zephyrhills, Florida, United States
Santarus Clinical Investigational Site 5090
🇺🇸Annapolis, Maryland, United States
Santarus Clinical Investigational Site 5008
🇺🇸Metairie, Louisiana, United States
Santarus Clinical Investigational Site 5092
🇺🇸Hollywood, Maryland, United States
Santarus Clinical Investigational Site 5078
🇺🇸Dayton, Ohio, United States
Santarus Clinical Investigational Site 5096
🇺🇸Fayetteville, North Carolina, United States
Santarus Clinical Investigational Site 5091
🇺🇸New Bern, North Carolina, United States
Santarus Clinical Investigational Site 5065
🇺🇸Pottstown, Pennsylvania, United States
Santarus Clinical Investigational Site 5001
🇺🇸Yukon, Oklahoma, United States
Santarus Clinical Investigational Site 5066
🇺🇸Duncansville, Pennsylvania, United States
Santarus Clinical Investigational Site 6014
🇨🇦Vancouver, British Columbia, Canada
Santarus Clinical Investigational Site 5032
🇺🇸Tampa, Florida, United States
Santarus Clinical Investigational Site 5009
🇺🇸Tampa, Florida, United States
Santarus Clinical Investigational Site 5100
🇺🇸San Antonio, Texas, United States
Santarus Clinical Investigational Site 5079
🇺🇸San Antonio, Texas, United States
Santarus Clinical Investigational Site 5015
🇺🇸Salt Lake City, Utah, United States
Santarus Clinical Investigational Site 5021
🇺🇸Austin, Texas, United States
Santarus Clinical Investigational Site 5005
🇺🇸Marlton, New Jersey, United States