Pharmacokinetics of Adalimumab With Methotrexate for Treatment of Patients With Ulcerative Colitis (UC)
- Sponsor
- Alimentiv Inc.
- Study ID
- NCT01716039
- Phase
- PHASE2
- Status
- Terminated
Conditions
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - 65 Years
- Healthy Volunteers
- Not accepted
Interventions
- MTX 12.5 — DRUGonce weekly oral dosing with MTX 12.5 mg (n=40) two weeks prior to the initiation of adalimumab. Randomization will be stratified by disease activity (modified Mayo Score ≤9 or \>9). Subjects will receive 18 weekly doses of MTX in addition to doses of adalimumab
- MTX 25 — DRUGonce weekly oral dosing with MTX 25 mg (n=40) two weeks prior to the initiation of adalimumab. Randomization will be stratified by disease activity (modified Mayo Score ≤9 or \>9). Subjects will receive 18 weekly doses of MTX in addition to doses of adalimumab
- Adalimumab — DRUGSubjects will receive 18 weekly doses of adalimumab
Study Details
Assess the body's reaction to dose-response relationship for the adalimumab/Methotrexate interaction in subjects with moderately to severely active ulcerative colitis.
Key Dates
- Start date
- Jun 30, 2013
- Status verified
- Jun 2021
- Primary completion
- Jul 18, 2016
- Completion
- Jul 18, 2016
Study Design
- Enrollment
- 22 participants (actual)
- Allocation
- RANDOMIZED
- Intervention model
- PARALLEL
- Primary purpose
- TREATMENT
Arms
- Active Comparator: MTX 12.5Receive once weekly oral dosing with MTX 12.5 mg (n=40) two weeks prior to the initiation of adalimumab 18 weekly doses of MTX and/or placebo in addition to doses of adalimumab
- Active Comparator: MTX 25 mgOnce weekly oral dosing with MTX 25 mg (n=40) two weeks prior to the initiation of adalimumab 18 weekly doses of MTX in addition to doses of adalimumab
- Placebo Comparator: PlaceboOnce weekly oral dosing with placebo (n=20) two weeks prior to the initiation of adalimumab. Subjects will receive 18 weekly doses of placebo in addition to doses of adalimumab
Primary Outcome Measure
Change in the Modified Baron Score From Baseline to the Final Visit (Week 18) Between the Treatment Groups [ Time Frame: Baseline up to Week 18 ]
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