Loading clinical trials...
Loading clinical trials...
Clinical Pharmacological Study of FYU-981 Administered to Hyperuricemic Outpatients With or Without Gout
To investigate the pharmacodynamics and safety of FYU-981 administered orally once a day for 14 weeks, to uric acid-overproduction type or uric acid-underexcretion type of male hyperuricemic outpatients with or without gout.
Age
20 - No limit years
Sex
MALE
Healthy Volunteers
No
Mochida Investigational sites
Tokyo, Japan
Start Date
January 4, 2018
Primary Completion Date
May 29, 2018
Completion Date
June 5, 2018
Last Updated
September 24, 2018
26
ACTUAL participants
FYU-981
DRUG
Lead Sponsor
Mochida Pharmaceutical Company, Ltd.
Collaborators
Data Source & Attribution
This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.
Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.
Neither the United States Government nor Clareo Health make any warranties regarding the data. Check ClinicalTrials.gov frequently for updates.
View ClinicalTrials.gov Terms and Conditions