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Clinical Trial Summary

An open label, balanced, randomised, four-treatment, four-period, four-sequence, single oral dose, crossover Pharmacokinetics study of WD-1603 carbidopa/levodopa extended-release tablets in normal, healthy, adult human subjects under fed conditions. A single oral dose of (either Treatment A or B or C or D) carbidopa/levodopa extended release tablets will be administered to each subject within 5 minutes after completion of standardized vegetarian breakfast under fed condition in each period as per randomization schedule.


Clinical Trial Description

This is an open label, balanced, randomised, four-treatment, four-period, four-sequence, single oral dose, crossover Pharmacokinetics study of WD-1603 carbidopa/levodopa extended-release tablets in normal, healthy, adult human subjects under fed conditions. A single oral dose of (either Treatment A or B or C or D) carbidopa/levodopa extended release tablets will be administered to each subject within 5 minutes after completion of standardized vegetarian breakfast under fed condition in each period as per randomization schedule. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04591535
Study type Interventional
Source Hong Kong WD Pharmaceutical Co., Limited
Contact Xiaoxiong Wei, Doctor
Phone +86-21-6859-9718
Email [email protected]
Status Recruiting
Phase Phase 1
Start date September 28, 2020
Completion date March 28, 2021

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