MedPath

Study of absorption and elimination rate of Linagliptin tablets 5 mg in comparison with Linagliptin brand tablets (Tradjenta®).

Not Applicable
Not yet recruiting
Conditions
Bioequivalence study.
Registration Number
IRCT20200407046981N37
Lead Sponsor
Darmanyab darou pharmaceutical company
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Pending
Sex
Male
Target Recruitment
24
Inclusion Criteria

The weight limit of each volunteer should be between 60 and 100 kg.
All volunteers must be non-smokers.
They must be healthy in terms of liver, kidney, respiratory system, mental and other general health characteristics that will be assessed.
Candidates who have consented to the consent form.

Exclusion Criteria

Known hypersensitivity or idiosyncratic reaction to Linagliptin or any ingredients.
Subjects with BP = 90/60 mm/Hg or BP = 140/90 mm/Hg.
Regular smoker who smokes more than ten cigarettes daily.
Taking any medicine during two weeks before dosing.

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod

MedPath

Empowering clinical research with data-driven insights and AI-powered tools.

© 2025 MedPath, Inc. All rights reserved.