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Sponsors and Collaborators: |
Wyeth Progenics Pharmaceuticals, Inc. |
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Information provided by: | Wyeth |
ClinicalTrials.gov Identifier: | NCT00605644 |
The primary purpose of this study is to evaluate the safety and dose-response relationship of N-methylnaltrexone bromide (MOA-728) by observing spontaneous bowel movements in subjects administered MOA-728 who have chronic pain that is not due to cancer, and who have opioid-induced bowel dysfunction (OIBD).
Condition | Intervention | Phase |
---|---|---|
Constipation |
Drug: MOA-728 Drug: Placebo |
Phase II |
Study Type: | Interventional |
Study Design: | Treatment, Randomized, Double Blind (Subject, Investigator, Outcomes Assessor), Placebo Control, Parallel Assignment, Safety/Efficacy Study |
Official Title: | A Multicenter, Randomized, Double-Blind, Placebo-Controlled, Parallel-Group Study of Oral MOA-728 for the Treatment of Opioid-Induced Bowel Dysfunction in Subjects With Chronic Nonmalignant Pain |
Enrollment: | 120 |
Study Start Date: | January 2008 |
Study Completion Date: | May 2008 |
Primary Completion Date: | May 2008 (Final data collection date for primary outcome measure) |
Arms | Assigned Interventions |
---|---|
1: Placebo Comparator
Placebo
|
Drug: Placebo
Placebo
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2: Experimental
MOA-728
|
Drug: MOA-728
Oral Capsules
|
3: Experimental
MOA-728
|
Drug: MOA-728
Oral Capsules
|
4: Experimental
MOA-728
|
Drug: MOA-728
Oral Capsules
|
5: Experimental
MOA-728
|
Drug: MOA-728
Oral Capsules
|
Ages Eligible for Study: | 18 Years and older |
Genders Eligible for Study: | Both |
Accepts Healthy Volunteers: | No |
Inclusion Criteria:
Exclusion Criteria:
Responsible Party: | Wyeth ( Wyeth (Registry Contact: Clinical Trial Registry Specialist) ) |
Study ID Numbers: | 3200A3-2202 |
Study First Received: | January 18, 2008 |
Last Updated: | August 13, 2008 |
ClinicalTrials.gov Identifier: | NCT00605644 |
Health Authority: | United States: Food and Drug Administration |
Signs and Symptoms Signs and Symptoms, Digestive Constipation Pain |