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)
View Full Details on ClinicalTrials.gov
For the most up-to-date information, visit the official listing.
NCT06431477
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