Clinical Trials Directory

Trials / Completed

CompletedNCT00080210

A Study of Persons With Gout Who Do Not Respond to or Are Allergic to Conventional Therapy

A Phase II Study of Multiple Doses of Intravenous Puricase in Subjects With Hyperuricemia and Refractory Gout

Status
Completed
Phase
Phase 2
Study type
Interventional
Enrollment
40 (planned)
Sponsor
Savient Pharmaceuticals · Industry
Sex
All
Age
18 Years – 90 Years
Healthy volunteers
Not accepted

Summary

This is a randomized, open-label, multicenter, parallel-groups study of multiple intravenous doses of Puricase, administered intravenously, in 40 patients with symptomatic gout. Subjects must wash out of any uric acid-lowering agents for one week before being dosed, and must refrain from using such agents throughout the study.

Conditions

Interventions

TypeNameDescription
DRUGPuricase

Timeline

Start date
2004-03-01
Completion
2005-02-01
First posted
2004-03-25
Last updated
2013-06-03

Locations

9 sites across 1 country: United States

Source: ClinicalTrials.gov record NCT00080210. Inclusion in this directory is not an endorsement.