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Pharmacokinetics of Irbesartan High/Amlodipine FDC and Co-administration of Irbesartan High and Amlodipine in Healthy Volunteers

Phase 1
Completed
Conditions
Healthy Volunteers
Interventions
Registration Number
NCT05688085
Lead Sponsor
Handok Inc.
Brief Summary

The purpose of this study is to compare pharmacokinetics and safety of Irbesartan High and Amlodipine Fixed Dose Combination and coadministration of mono compounds in healthy adult volunteers

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
44
Inclusion Criteria
  • Patients who are 19 years or older on screening
  • Signed informed consent
  • Healthy Volunteer
  • Other inclusion applied
Exclusion Criteria
  • Clinically relevant/significant findings as evaluated by the investigator
  • Other exclusion applied

Study & Design

Study Type
INTERVENTIONAL
Study Design
CROSSOVER
Arm && Interventions
GroupInterventionDescription
Co-administration of Irbesartan High and AmlodipineAmlodipineparticipants will receive one table each of Irbesartan High and Amlodipine in a crossover design
Irbesartan High/Amlodipine Fixed dose combinationIrbesartan High/Amlodipine FDCparticipants will receive one tablet of Irbesartan High/Amlodipine FDC in a crossover design
Co-administration of Irbesartan High and AmlodipineIrbesartan Highparticipants will receive one table each of Irbesartan High and Amlodipine in a crossover design
Primary Outcome Measures
NameTimeMethod
AUCt of Irbesartan High and Amlodipine72 hours
Cmax of Irbesartan High and Amlodipine72 hours
Secondary Outcome Measures
NameTimeMethod
AUCinf of Irbesartan High and Amlodipine72 hours
tmax of Irbesartan High and Amlodipine72 hours
Vz/F of Irbesartan High and Amlodipine72 hours
AUCt/AUCinf of Irbesartan High and Amlodipine72 hours
half-life of Irbesartan High and Amlodipine72 hours
CL/F of Irbesartan High and Amlodipine72 hours

Trial Locations

Locations (1)

H Plus Yangji Hospital

🇰🇷

Seoul, Korea, Republic of

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