Study Evaluating the Safety of MOA-728 Administered Orally to Healthy Subjects
Completed · Phase 1
Conditions studied: Postoperative Complications, Constipation
In brief
This is the first multiple-dose experience in humans with MOA-728 in an oral formulation. This study will provide an assessment of the safety, tolerability, and pharmacokinetics (PK) of MOA-728 following administration of ascending multiple oral doses to healthy subjects.
Key facts
- Study ID
- NCT00311350
- Run by
- Bausch Health Americas, Inc.
- People needed
- 48
- Starts
- 2006-03-01
- Expected to finish
- 2006-08-01
- Last updated by the study team
- 2019-11-25
Who can join
Age: 18 and older, up to 50. Sex: any. Healthy volunteers: accepted.
You may qualify if…
- Healthy men and women
Where it is running
- Study site — Philadelphia, Pennsylvania, United States
Full record on ClinicalTrials.gov
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