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
| Type | Name | Description |
|---|---|---|
| DRUG | Eletriptan commercial tablet | 20 mg tablet, single dose |
| DRUG | Eletriptan commercial tablet | 40 mg tablet, single dose of 1 X 40 mg |
| DRUG | Eletriptan commercial tablet | 40 mg tablet, single dose of 2 X 40 mg |
| DRUG | Eletriptan commercial tablet | 40 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.