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NCT03032315

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

Completed Phase 1 Last updated 26 January 2017
What this trial tests

Phase 1 trial testing TAH Tablet (Telmisartan80/Amlodipine besylate10/Hydrochlorothiazide12.5) in Healthy in 44 participants. Completed in 27 December 2016.

Timeline
1 October 2016
Primary endpoint
27 December 2016
27 December 2016

Quick facts

Lead sponsorIlDong Pharmaceutical Co Ltd
PhasePhase 1
StatusCompleted
Study typeINTERVENTIONAL
Allocationrandomized
Designcrossover
Maskingnone
Primary purposetreatment
Enrollment44
Start date1 October 2016
Primary completion27 December 2016
Estimated completion27 December 2016
Sites1 location across South Korea

Drugs / interventions tested

Conditions studied

Sponsor

IlDong Pharmaceutical Co Ltd — full company profile →

Who can join

Adults 19 to 55, male only, with Healthy. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

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

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

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Other recruiting trials for Healthy

Currently open trials in the same condition.

Other IlDong Pharmaceutical Co Ltd trials

Trials by the same sponsor.

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Data sources for this page

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