Clinical Trials Directory

Trials / Completed

CompletedNCT03032315

Compare the Pharmacokinetics of TAH(80/10/12.5) Tablet in Comparison to the Co-administration of Telmisartan, Amlodipine and Hydrochlorothiazide in Healthy Male Volunteers

Clinical Trial to Compare the Pharmacokinetics of TAH Tablet(80/10/12.5mg) in Comparison to the Co-administration of Telmisartan, Amlodipine and Hydrochlorothiazide in Healthy Male Volunteers

Status
Completed
Phase
Phase 1
Study type
Interventional
Enrollment
44 (actual)
Sponsor
IlDong Pharmaceutical Co Ltd · Industry
Sex
Male
Age
19 Years – 55 Years
Healthy volunteers
Accepted

Summary

randomized, open-label, single dose, replicate crossover clinical trial to compare the pharmacokinetics of TAH(80/10/12.5) tablet in comparison to the co-administration of telmisartan, amlodipine and hydrochlorothiazide in healthy male volunteers

Conditions

Interventions

TypeNameDescription
DRUGTAH Tablet (Telmisartan80/Amlodipine besylate10/Hydrochlorothiazide12.5)Telmisartan 80.0 mg, Amlodipine besylate 13.87 mg (Amlodipine 10 mg), Hydrochlorothiazide 12.5 mg combination-drug would be administered orally once
DRUGTWYNSTA(Telmisartan+Amlodipine besylate)TWYNSTA 2 Tab. 40/5mg(Telmisartan 40 mg, Amlodipine besylate 6.935 mg(Amlodipine 5 mg) would be administered orally once
DRUGHydrochlorothiazideDichlozid 1 Tab.(Hydrochlorothiazide 12.5 mg) would be administered orally once

Timeline

Start date
2016-10-01
Primary completion
2016-12-27
Completion
2016-12-27
First posted
2017-01-26
Last updated
2017-01-26

Locations

1 site across 1 country: South Korea

Source: ClinicalTrials.gov record NCT03032315. Inclusion in this directory is not an endorsement.