Clinical Trials Directory

Trials / Completed

CompletedNCT01806311

Safety and Pharmacokinetics Study of amlodipine10mg and candesartan32mg

An Open-label, Multiple-dose, Two-arm, One-sequence, Crossover Study to Evaluate the Safety and Pharmacokinetics After Oral Concurrent Administration of amlodipine10mg and candesartan32mg in Healthy Male Volunteers

Status
Completed
Phase
Phase 1
Study type
Interventional
Enrollment
36 (actual)
Sponsor
HanAll BioPharma Co., Ltd. · Industry
Sex
Male
Age
20 Years – 45 Years
Healthy volunteers
Accepted

Summary

Clinical trial to evalate the pharmacokinetic interactions and safety between single dose of amlodipine10mg and candesartan32mg and combiation dose amlodipine10mg with candesartan32mg in healthy male volunteers.

Conditions

Interventions

TypeNameDescription
DRUGCandesartan32mg
DRUGAmlodipine10mg

Timeline

Start date
2012-12-01
Primary completion
2013-08-01
Completion
2013-08-01
First posted
2013-03-07
Last updated
2025-04-20

Locations

1 site across 1 country: South Korea

Source: ClinicalTrials.gov record NCT01806311. Inclusion in this directory is not an endorsement.

Safety and Pharmacokinetics Study of amlodipine10mg and candesartan32mg (NCT01806311) · Clinical Trials Directory