The purpose of this study is to evaluate the bioequivalence of the test formulation and reference formulation of cabergoline tablets in healthy Chinese subjects under fasting and postprandial conditions.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
OTHER
Masking
NONE
Enrollment
72
Single oral administration
Single oral administration
Zhejiang Xiaoshan Hospital
Hangzhou, Zhejiang, China
Cmax
Time frame: : 0 hours-72 hours post-administration
AUC0-72h
Time frame: 0 hours-72 hours post-administration
This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.