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CompletedNCT01366352

Pharmacokinetics and Bioavailability Comparison of Two Different Formulations of MNTX Tablets

Pharmacokinetics and Bioavailability Comparison of Two Different Formulations of MNTX Tablets: A Double-Blind, Single Dose, Crossover, Phase 1 Study in Normal Volunteers

Status
Completed
Phase
Phase 1
Study type
Interventional
Enrollment
24 (actual)
Sponsor
Bausch Health Americas, Inc. · Industry
Sex
All
Age
18 Years – 45 Years
Healthy volunteers
Accepted

Summary

This was a single-center, double-blind, randomized, cross-over Phase 1 study in normal, healthy volunteers. Study treatment entailed single doses of two different formulations of MNTX tablets.

Conditions

Interventions

TypeNameDescription
DRUGMNTX tablet (Formulation 1)
DRUGMNTX tablet (Formulation 2)

Timeline

Start date
2004-02-01
Primary completion
2004-03-01
Completion
2004-03-01
First posted
2011-06-06
Last updated
2019-11-27

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT01366352. Inclusion in this directory is not an endorsement.

Pharmacokinetics and Bioavailability Comparison of Two Different Formulations of MNTX Tablets (NCT01366352) · Clinical Trials Directory