Viewing Study NCT00080210



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Last Modification Date: 2024-10-26 @ 9:10 AM
Study NCT ID: NCT00080210
Status: COMPLETED
Last Update Posted: 2013-06-03
First Post: 2004-03-24

Brief Title: A Study of Persons With Gout Who Do Not Respond to or Are Allergic to Conventional Therapy
Sponsor: Savient Pharmaceuticals
Organization: Savient Pharmaceuticals

Study Overview

Official Title: A Phase II Study of Multiple Doses of Intravenous Puricase in Subjects With Hyperuricemia and Refractory Gout
Status: COMPLETED
Status Verified Date: 2013-05
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: No
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief 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
Detailed Description: None

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: None
Is a FDA Regulated Device?: None
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None