Clinical Trials Directory

Trials / Completed

CompletedNCT01139515

Eletriptan Pharmacokinetics In Korean Males

An Open Label, Single And Repeat Dose Randomized Crossover Study To Estimate The Pharmacokinetics And Safety Of Eletriptan Hydrobromide Tablets In Healthy Korean Male Subjects

Status
Completed
Phase
Phase 1
Study type
Interventional
Enrollment
16 (actual)
Sponsor
Pfizer's Upjohn has merged with Mylan to form Viatris Inc. · Industry
Sex
Male
Age
18 Years – 55 Years
Healthy volunteers
Accepted

Summary

The hypothesis of this study is that Korean subjects have similar Pharmacokinetics (PK) characteristics to those seen in other populations.

Conditions

Interventions

TypeNameDescription
DRUGEletriptan commercial tablet20 mg tablet, single dose
DRUGEletriptan commercial tablet40 mg tablet, single dose of 1 X 40 mg
DRUGEletriptan commercial tablet40 mg tablet, single dose of 2 X 40 mg
DRUGEletriptan commercial tablet40 mg tablet, 1 X 40 mg given two times: the second 2 hours after the first

Timeline

Start date
2010-07-01
Primary completion
2010-07-01
Completion
2010-07-01
First posted
2010-06-08
Last updated
2021-01-28
Results posted
2011-07-12

Locations

1 site across 1 country: South Korea

Source: ClinicalTrials.gov record NCT01139515. Inclusion in this directory is not an endorsement.