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CompletedNCT02524678

Phase 1 Study(Additional) of URC102 in Healthy Subjects

A Phase I, Placebo-controlled, Randomized, Double Blind, Dose-escalation Study to Assess the Safety and Pharmacokinetic and Pharmacodynamic Characteristics of Repeated-dose URC102 in Healthy Korean Adult Males

Status
Completed
Phase
Phase 1
Study type
Interventional
Enrollment
21 (actual)
Sponsor
JW Pharmaceutical · Industry
Sex
Male
Age
20 Years – 49 Years
Healthy volunteers
Accepted

Summary

The purpose of this study is to assess the safety, tolerability, PK and PD of URC102 in healthy subjects.

Detailed description

Tolerability, safety, and pharmacokinetics (PK) of URC102 will be assessed after 7-day repeated oral dose in healthy adult Korean males. In addition, pharmacodynamic (PD) response of blood and urinary uric acid levels will be assessed.

Conditions

Interventions

TypeNameDescription
DRUGPlacebo
DRUGURC102

Timeline

Start date
2015-08-05
Primary completion
2015-10-07
Completion
2016-03-28
First posted
2015-08-17
Last updated
2020-02-13

Locations

1 site across 1 country: South Korea

Source: ClinicalTrials.gov record NCT02524678. Inclusion in this directory is not an endorsement.

Phase 1 Study(Additional) of URC102 in Healthy Subjects (NCT02524678) · Clinical Trials Directory