Assessing the Safety/Efficacy of Asacol® Given Every 12 Hours to Children and Adolescents for the Maintenance of Remission of Ulcerative Colitis (CAMPIII)
Tracking InformationStart Date ICMJE | October 2009 |
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Estimated Primary Completion Date | May 2012 (final data collection date for primary outcome measure) |
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Current Primary Outcome Measures ICMJE (submitted: October 28, 2009) | proportion of patients who have maintained complete remission through Week 26 as determined by a Pediatric Ulcerative Colitis Activity Index (PUCAI) score < 10 during the entire study period [ Time Frame: Week 26 ] [ Designated as safety issue: No ] |
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Original Primary Outcome Measures ICMJE | Same as current |
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Change History | Complete list of historical versions of study NCT01004185 on ClinicalTrials.gov Archive Site |
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Current Secondary Outcome Measures ICMJE (submitted: October 28, 2009) | proportion of patients who have maintained complete remission through Week 26 using an endpoint similar to the PUCAI (but with the PUCAI 3-level Abdominal Pain question replaced by a 5-level Abdominal Pain question) [ Time Frame: Week 26 ] [ Designated as safety issue: No ] |
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Original Secondary Outcome Measures ICMJE | Same as current |
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Descriptive InformationBrief Title ICMJE | Assessing the Safety/Efficacy of Asacol® Given Every 12 Hours to Children and Adolescents for the Maintenance of Remission of Ulcerative Colitis |
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Official Title ICMJE | A Randomized, Double-blind, Parallel-group Study to Assess the Safety and Efficacy of Asacol® (1.2 to 4.8g/Day) 400 mg Delayed-release Tablets Given Twice Daily for 26 Weeks to Children and Adolescents for the Maintenance of Remission of Ulcerative Colitis |
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Brief Summary | The purpose of this study is to determine whether low dose Asacol® (27 mg/kg - 71 mg/kg) and high dose Asacol® (53 mg/kg - 118 mg/kg) are safe and effective when dosed as 400 mg delayed-release tablets given twice daily for 26 weeks to children and adolescents for the maintenance of remission of ulcerative colitis. |
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Detailed Description | |
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Study Phase | Phase III |
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Study Type ICMJE | Interventional |
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Study Design ICMJE | Treatment, Randomized, Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor), Dose Comparison, Parallel Assignment, Safety/Efficacy Study |
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Condition ICMJE | Ulcerative Colitis |
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Intervention ICMJE | - Drug: Asacol (mesalamine), High Dose
Patients will be randomized at baseline to high and low dose Asacol and stratified by weight. Subjects randomized to receive High Dose who weigh 17-<33 kg will receive 3 Asacol 400mg tablets in morning and 2 Asacol 400 tablets in PM. Subjects randomized to receive High Dose who weigh 33-<54 kg will receive 5 Asacol 400mg tablets in morning and 4 Asacol 400 tablets in PM. Subjects randomized to receive High Dose who weigh 54-<90 kg will receive 6 Asacol 400mg tablets in morning and 6 Asacol 400 tablets in PM. Other Name: Asacol; mesalamine; 5-aminosalicylic acid; 5-ASA; mesalazine - Drug: Asacol (mesalamine), Low Dose
Patients will be randomized at baseline to high and low dose Asacol and stratified by weight. Subjects randomized to receive Low Dose who weigh 17-<33 kg will receive 2 Asacol 400mg tablets + 1 placebo tablet in morning and 1 Asacol 400 tablet +1 placebo tablet in PM. Subjects randomized to receive Low Dose who weigh 33-<54 kg will receive 3 Asacol 400mg tablets +2 placebo tablets in morning and 2 Asacol 400 tablets + 2 placebo tablets in PM. Subjects randomized to receive Low Dose who weigh 54-<90 kg will receive 3 Asacol 400mg tablets + 3 placebo tablets in morning and 3 Asacol 400mg tablets + 3 placebo tablets in PM. Other Name: Asacol; mesalamine; 5-aminosalicylic acid; 5-ASA; mesalazine
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Study Arms / Comparison Groups | - High Dose: Experimental
Subjects who weigh 17-<33 kg will receive 2.0 g/day Asacol. Subjects who weigh 33-<54 kg will receive 3.6 g/day Asacol. Subjects who weigh 54-<90 kg will receive 4.8 g/day Asacol. Intervention: Drug: Asacol (mesalamine), High Dose - Low Dose: Experimental
Subjects who weigh 17-<33 kg will receive 1.2 g/day Asacol. Subjects who weigh 33-<54 kg will receive 2.0 g/day Asacol. Subjects who weigh 54-<90 kg will receive 2.4 g/day Asacol. Intervention: Drug: Asacol (mesalamine), Low Dose
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Recruitment InformationEstimated Enrollment ICMJE | 100 |
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Estimated Completion Date | May 2012 |
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Estimated Primary Completion Date | May 2012 (final data collection date for primary outcome measure) |
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Eligibility Criteria ICMJE | Inclusion Criteria: - male or female between the ages of 5 and 17 years, inclusive, at the time of the first dose of study medication;
- have a documented history of UC that has been successfully maintained in complete remission for at least 1 month prior to study entry
- have a baseline PUCAI score < 10
- have a body weight no less than 17 kg and no more than 90 kg
- have a history of at least 1 active episode or relapse in the last 12 months
- have taken a stable maintenance dose of oral mesalamine (or equivalent oral 5-ASA dose) for at least 1 month prior to entry in the study. Stable is defined as the same dose for the last month.
- maintained complete remission, as defined, throughout the 30-day run-in phase. Note:ONLY applies to those patients who complete the 6-week treatment in complete remission from Study 2007017 and immediately roll-over to the 30-day run-in phase
- are female patients who are pre-menarchal or have a negative urine pregnancy test and, if sexually active, practice acceptable contraception (e.g., abstinence; oral, intramuscular, or implanted hormonal contraception [at least 3 months prior to enrollment]
Exclusion Criteria: - have a history of allergy or hypersensitivity to salicylates, aminosalicylates, or any component of the Asacol tablet
- have a significant co-existing illness or other condition(s), including but not limited to cancer or significant organic or psychiatric disease on medical history or physical examination, that, in the judgment of the Investigator, contraindicate(s) administration of the study drug and/or any study procedures
- have a history or presence of any condition causing malabsorption or an effect on gastrointestinal motility or history of extensive small bowel resection (greater than one half the length of the small intestine) causing short bowel syndrome
- any "condition" causing "malabsorption" or an effect on gastrointestinal "motility"
- have current renal disease, or a screening blood urea nitrogen (BUN) or creatinine value that is > 1.5 times the upper limit of the age appropriate normal
- have a documented history of or current hepatic disease, or liver function tests (alanine transaminase [ALT], aspartate transaminase [AST], total bilirubin) that are > 2 times the upper limit of normal
- have a history of pancreatitis
- have undergone treatment with any oral, intravenous, intramuscular, or rectally administered corticosteroids (including budesonide) within 30 days prior to the Screening visit
- have undergone treatment with any rectal mesalamine therapy within 30 days prior to the screening visit
- have undergone treatment with immunomodulatory therapy including, but not limited to: rosiglitazone, 6-mercaptopurine or azathioprine, cyclosporine, or methotrexate within 90 days prior to Screening visit
- have undergone treatment with biologic therapy including, but not limited to: infliximab,adalimumab, certolizumab or other biologic treatment of ulcerative colitis within 90 days prior to Screening visit
- have undergone treatment with antibiotics (other than topical antibiotics) including metronidazole within 7 days prior to the Screening visit
- have undergone treatment with aspirin or other nonsteroidal anti-inflammatory drugs NSAIDs) within 7 days prior to the Screening visit
- have undergone treatment with any antidiarrheals and/or antispasmodics within 30 days of the Screening visit
- have a stool examination positive for Clostridium difficile (C. difficile), bacterial pathogens, or ova and parasites. Note: Because normal gut flora may vary by geography, the Medical Monitor should be consulted before excluding a patient with a stool sample that is positive for C. difficile, bacterial pathogens or ova and parasites.
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Gender | Both |
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Ages | 5 Years to 17 Years |
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Accepts Healthy Volunteers | No |
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Contacts ICMJE | |
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Location Countries ICMJE | United States, Canada, Croatia, Poland, Romania, Russian Federation |
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Administrative InformationNCT ID ICMJE | NCT01004185 |
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Responsible Party | Preston Dunnmon, MD, Procter & Gamble Pharmaceuticals |
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Study ID Numbers ICMJE | 2008085 |
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Study Sponsor ICMJE | Procter and Gamble |
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Collaborators ICMJE | |
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Investigators ICMJE | |
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Information Provided By | Procter and Gamble |
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