Overview

Comparative Pharmacokinetic Study of Aprepitant Injection in Humans

Status:
NOT_YET_RECRUITING
Trial end date:
2025-01-25
Target enrollment:
Participant gender:
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.
Phase:
PHASE1
Details
Lead Sponsor:
The Affiliated Hospital of Qingdao University
Treatments:
Aprepitant