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NCT00311350 Clinical Trial

Study Evaluating the Safety of MOA-728 Administered Orally to Healthy Subjects

Postoperative Complications Clinical Trial

Official title:
Ascending Multiple Dose Study of the Safety, Tolerability, and Pharmacokinetics of MOA-728 Administered Orally to Healthy Subjects

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT00311350
Other study ID # 3200A3-100
Secondary ID
Status Completed
Phase Phase 1
First received
Last updated
Start date March 2006
Est. completion date August 2006

Study information
Verified date November 2019
Source Bausch Health Americas, Inc.
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

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.

Recruitment information / eligibility
Status Completed
Enrollment 48
Est. completion date August 2006
Est. primary completion date
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 50 Years
Eligibility Inclusion Criteria:

- Healthy men and women

Study Design

Related Conditions & MeSH terms

Intervention

Drug:
• MOA-728

Locations
Country Name City State
n/a

Sponsors (1)
Lead Sponsor Collaborator
Bausch Health Americas, Inc.

Country where clinical trial is conducted

United States, 

Outcome
Type Measure Description Time frame Safety issue
Primary Safety
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