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CKD-828 (80/5mg) Pharmacokinetic Study

NCT02250833 · Status: COMPLETED · Phase: PHASE1 · Type: INTERVENTIONAL · Enrollment: 69

Last updated 2015-04-10

No results posted yet for this study

Summary

A randomized, open-label, single-dose, two-period, two-way, crossover study to compare the pharmacokinetics and safety CKD-828 (Fixed Dose Combination Tablet) to coadministration telmisartan and s-amlodipine in health volunteers.

Conditions

Interventions

DRUG

CKD-828

Telmisartan 80mg /S-Amlodipine 5mg(FDC) Tablet, Oral, Once Daily

DRUG

Telmisartan

\- Telmisartan 80mg tablet, Oral, Once Daily (Combination Therapy with S-amlodipine)

DRUG

S-amlodipine

\- S-amlodipine 5mg tablet, Oral, Once Daily (combination Therapy with Telmisartan)

Sponsors & Collaborators

  • Chong Kun Dang Pharmaceutical

    lead INDUSTRY

Principal Investigators

  • Young-Ran Yoon · Kyungpook National University Hospital Clinical Trial Center

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
CROSSOVER

Eligibility

Min Age
19 Years
Max Age
55 Years
Sex
MALE
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2014-09-30
Primary Completion
2014-12-31
Completion
2014-12-31

Countries

  • South Korea

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Entities

Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02250833 on ClinicalTrials.gov