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Sponsored by: |
Wyeth |
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Information provided by: | Wyeth |
ClinicalTrials.gov Identifier: | NCT00398502 |
Primary: To determine the relative bioavailability of MOA-728, an investigational drug, administered orally in both the capsule and tablet formulations to methadone maintenance subjects.Secondary: To assess the pharmacodynamic effect of MOA-728 administered both orally and subcutaneously to methadone maintenance subjects using the oral-cecal transit time.
Condition | Intervention | Phase |
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Metahdone-Maintenance Subjects |
Drug: MOA-728 |
Phase I |
Study Type: | Interventional |
Study Design: | Treatment, Randomized, Open Label, Uncontrolled, Crossover Assignment, Bio-availability Study |
Official Title: | A Randomized, Open-Label, 3-Period Crossover Study to Determine the Relative Bioavailability of Two Oral Formulations of MOA-728 and to Compare the Pharmacodynamics of the Two Oral Formulations of MOA-728 and the Subcutaneous Formulation in Subjects on Stable Methadone Maintenance |
Ages Eligible for Study: | 18 Years to 65 Years |
Genders Eligible for Study: | Both |
Accepts Healthy Volunteers: | No |
Study ID Numbers: | 3200A3-105 |
Study First Received: | November 9, 2006 |
Last Updated: | December 3, 2007 |
ClinicalTrials.gov Identifier: | NCT00398502 History of Changes |
Health Authority: | United States: Food and Drug Administration |
Methadone |