RecruitingPhase 4NCT06431477

Efficacy and Safety of Telmisartan Compared With Losartan

A Multi-center, Randomized, Open-label, Active Comparator-controlled, Phase 4 Clinical Trial To Evaluate the Efficacy and Safety of Telmisartan Compared With Losartan in Patients With Diabetic Nephropathy and Hypertension


Sponsor

Chong Kun Dang Pharmaceutical

Enrollment

98 participants

Start Date

Apr 19, 2023

Study Type

INTERVENTIONAL

Conditions

Summary

A study to evaluate the efficacy and safety of telmisartan compared with losartan in patients with diabetic nephropathy and hypertension


Eligibility

Min Age: 19 YearsMax Age: 75 Years

Inclusion Criteria3

  • Male of Female subjects aged ≥19 or \<75
  • Type II Diabetes Mellitus subjects who have been taken medicine
  • Subjects who have voluntarily decided to participate in this clinical trial and Signed ICF

Exclusion Criteria6

  • Subjects with Type I Diabetes Mellitus
  • Subjects with Primary hyper-aldosteronism
  • Subjects with a history of drug or alcohol abuse or suspected patient within 1 year as of the time of screening
  • Pregnant women, lactating women, or subjects who do not agree to use appropriate contraception during the clinical trial period
  • Subjects who received other clinical trial drugs within 28 days of screening visit
  • Subjects who are unable to participate in this clinical trial at the discretion of the investigator.

Interventions

DRUGtelmisartan

QD, PO

DRUGLosartan

QD, PO


Locations(1)

Severance Hospital

Seoul, South Korea

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NCT06431477


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