An Open-label, Rendomized, Single-dose Crossover Study to Evaluate the Pharmacokinetics, Safety and Tolerability of CKD-387 in Healthy Subjects
Abstract
The purpose of this study is to evaluate the pharmacokinetics, safety and tolerability of CKD-387
Conditions: Type2 Diabetes Mellitus.
Primary outcome: Part A : Cmax under fasting condition; Part A : Cmax under fasting condition; Part A : AUClast under fasting condition; Part A : AUClast under fasting condition; Part B : Cmax under fed condition; Part B : AUClast under fed condition.
Enrollment: 58 participants.
How strong is the evidence?
Evidence Hub reads this as a clinical trial, done in people. Its evidence level is 3 of 5 (Moderate · trial / cohort / secondary analysis). Trials without a large randomized design, cohorts and secondary analyses give moderate evidence. Reported size: 58 participants or records.
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