Clinical Trials Directory

Trials / Completed

CompletedNCT01107353

Bioequivalency Study of Imipramine Pamoate 75 mg Capsules Under Fasted Conditions

A Single Dose, 2-Period, 2-Treatment, 2-Way Crossover Bioequivalency Study of Imipramine Pamoate Capsules, 75 mg, Under Fasted Conditions

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
39 (actual)
Sponsor
Roxane Laboratories · Industry
Sex
All
Age
18 Years – 45 Years
Healthy volunteers
Accepted

Summary

The objective of this study was to prove the bioequivalence of Imipramine Pamoate 75 mg Capsules under fasting conditions

Conditions

Interventions

TypeNameDescription
DRUGImipramine Pamoate75 mg capsule

Timeline

Start date
2008-08-01
Primary completion
2008-09-01
Completion
2008-09-01
First posted
2010-04-20
Last updated
2018-02-05
Results posted
2014-01-15

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT01107353. Inclusion in this directory is not an endorsement.

Bioequivalency Study of Imipramine Pamoate 75 mg Capsules Under Fasted Conditions (NCT01107353) · Clinical Trials Directory