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Completed Phase 3 Interventional Results available

Open-Label Extension Study for Patients Who Completed a Phase 3 Double-blind Study of PEG-uricase for Symptomatic Gout

ClinicalTrials.gov ID: NCT01356498

Public ClinicalTrials.gov record NCT01356498. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Jul 23, 2026, 6:59 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

Multicenter, Open Label Extension Study of 8 mg PEG-uricase in Subjects Who Completed Protocols C0405 or C0406 for Symptomatic Gout

Study identification

NCT ID
NCT01356498
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Savient Pharmaceuticals
Industry
Enrollment
151 participants

Conditions and interventions

Conditions

Interventions

  • pegloticase Biological

Biological

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Nov 30, 2006
Primary completion
Dec 31, 2009
Completion
Dec 31, 2009
Last update posted
Dec 1, 2011

2006 – 2010

United States locations

U.S. sites
22
U.S. states
13
U.S. cities
22
Facility City State ZIP Site status
Kaiser Permanente Medical Center, Clinical Trials Unit San Francisco California 94118
Pacific Arthritis Center Medical Group Santa Maria California 93454
Agilence Arthritis & Osteoporosis Medical Center Whittier California 90606
Veterans Affairs Medical Center Washington D.C. District of Columbia 20422
Arthritis & Rheumatic Disease Specialties Aventura Florida 33180
Ocala Rheumatology Research Center Ocala Florida 34474
St. Petersburg Arthritis Center St. Petersburg Florida 33703
The University of Chicago Chicago Illinois 60637
Graves Gilbert Clinic Bowling Green Kentucky 42101
Peter A. Holt, M.D. Baltimore Maryland 21239
Center for Rheumatology and Bone Research Wheaton Maryland 20902
Justus J. Fiechtner, MD, PC Lansing Michigan 48910
CentraCare Clinic Saint Cloud Minnesota 56377
Rheumatology Associates of North Jersey Teaneck New Jersey 07666
Duke University Medical Center Durham North Carolina 27302
New Horizons Clinical Research Cincinnati Ohio 45242
The Ohio State University Columbus Ohio 43210
STAT Research, Inc. Dayton Ohio 45402
David R. Mandel, MD, Inc. Mayfield Village Ohio 44143
Altoona Center for Clinical Research Duncansville Pennsylvania 16635
Mid Atlantic Research Assoc. Philadelphia Pennsylvania 19154
Arthritis Northwest, PLLC Spokane Washington 99204

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01356498, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Dec 1, 2011 · Synced Jul 23, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT01356498 live on ClinicalTrials.gov.

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