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Clinical Trial Summary

This is a single-center, open, randomized, single-dose, two-cycle, two-sequence, crossover pharmacokinetic study in healthy adult subjects. The trial is planned to enroll 24 healthy subjects. Subjects will be randomized to one of two groups (Group A: T-R, Group B: R-T) according to the randomization table. The washout period (dosing interval) between doses will be at least 7 days. For example, for a washout period of 7 days, all subjects will receive the appropriate drug according to the randomized schedule on Day 1 of Cycle 1 and Day 8 of Cycle 2 of the trial.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT06226506
Study type Interventional
Source The Affiliated Hospital of Qingdao University
Contact Yu Cao
Phone 18661809090
Email caoyu1767@126.com
Status Not yet recruiting
Phase Phase 1
Start date January 23, 2024
Completion date January 25, 2025

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