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CompletedNCT01146067

Bioequivalence Study of Rivastigmine 1.5 mg Capsules Under Fasting Conditions

Bioequivalence Study of Rivastigmine 1.5 mg Capsules (Test)of Dr.Reddy's Laboratories Limited Versus Exelon (Reference),Administered as 1 x 1.5 mg Capsule Under Fasting Conditions

Status
Completed
Phase
Phase 1
Study type
Interventional
Enrollment
44 (actual)
Sponsor
Dr. Reddy's Laboratories Limited · Industry
Sex
All
Age
18 Years
Healthy volunteers
Accepted

Summary

This is a bioequivalence study of Rivastigmine 1.5 mg capsules and Exelon Administered as 1.5 mg capsule in Healthy subjects under fasting conditions.

Detailed description

Single center, bioequivalence, open-label, randomized, 2-way crossover study administered as 1 x 1.5 mg capsule in healthy subjects under fasting conditions.

Conditions

Interventions

TypeNameDescription
DRUGRivastigmineRivastigmine capsules 1.5 mg

Timeline

Start date
2004-01-01
Primary completion
2004-02-01
Completion
2004-02-01
First posted
2010-06-17
Last updated
2012-01-13

Source: ClinicalTrials.gov record NCT01146067. Inclusion in this directory is not an endorsement.

Bioequivalence Study of Rivastigmine 1.5 mg Capsules Under Fasting Conditions (NCT01146067) · Clinical Trials Directory