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Compare the Pharmacokinetics of NVP-1205 and Coadministration of Rosuvastatin and Ezetimibe

A Clinical Trial to Compare the Pharmacokinetics and Safety of NVP-1205 and Coadministration of Rosuvastatin and Ezetimibe in Healthy Male Volunteers

Status
Completed
Phases
Phase 1
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02029625
Acronym
NVP-1205
Enrollment
41
Registered
2014-01-08
Start date
2014-02-28
Completion date
2014-03-31
Last updated
2016-03-25

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Dyslipidemia

Brief summary

The purpose of this study is to compare the pharmacokinetics of NVP-1205 and coadministration of rosuvastatin and ezetimibe.

Detailed description

rosuvastatin and ezetimibe(anti-dyslipidemia)

Interventions

DRUGNVP-1205

rosuvastatin/ezetimibe fixed dose combination orally, once daily on Period 1 or Period 2

coadministration of rosuvastatin and ezetimibe orally, once daily on Period 1 or Period 2

Sponsors

NVP Healthcare
Lead SponsorINDUSTRY

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
SCREENING
Masking
NONE

Eligibility

Sex/Gender
MALE
Age
19 Years to 55 Years
Healthy volunteers
Yes

Inclusion criteria

* Healthy male subjects age between 19 and 55 signed informed consent

Exclusion criteria

* subjects have a history of allergy reaction of this drug or other drugs

Design outcomes

Primary

MeasureTime frame
AUClast0-96hr

Secondary

MeasureTime frame
AUCinf0-96hr

Countries

South Korea

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 8, 2026