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Completed Phase 2 Interventional Results available

Long-term Efficacy, Safety and Tolerability of ACZ885 in Patients With Rheumatoid Arthritis

ClinicalTrials.gov ID: NCT00554606

Public ClinicalTrials.gov record NCT00554606. 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 Sep 4, 2026, 12:35 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

A 54-week, Phase II, Multi-center, Open-label Extension Study to Evaluate the Efficacy, Safety and Tolerability of ACZ885 (Anti-interleukin-1B Monoclonal Antibody) in Patients With Rheumatoid Arthritis

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

This study will assess the long-term safety and tolerability of ACZ885 in patients with rheumatoid arthritis, as well as long-term efficacy, long-term preservation and/or improvement of joint structure and bone mineral density, and long term maintenance of health-related quality of life.

Study identification

NCT ID
NCT00554606
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Novartis
Industry
Enrollment
115 participants

Conditions and interventions

Interventions

Drug

Eligibility (public fields only)

Age range
18 Years to 75 Years
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
Oct 10, 2007
Primary completion
Aug 12, 2009
Completion
Aug 12, 2009
Last update posted
Jul 8, 2021

2007 – 2009

United States locations

U.S. sites
20
U.S. states
13
U.S. cities
20
Facility City State ZIP Site status
Novartis Investigator Site Huntsville Alabama 35801
Novartis Investigator Site Tuscaloosa Alabama 35406
Novartis Investigator Site Paradise Valley Arizona 85253
Novartis Investigator Site Trumbull Connecticut 06611
Novartis Investigator Site Jacksonville Florida 32216
Novartis Investigator Site South Miami Florida 33143
Novartis Investigator Site Tamarac Florida 33321
Novartis Investigator Site Rockford Illinois 61107
Novartis Investigator Site Urbandale Indiana 50322
Novartis Investigator Site Richmond Heights Missouri 63117
Novartis Investigator Site Omaha Nebraska 68114
Novartis Investigator Site Reno Nevada 89502
Novartis Investigator Site Tulsa Oklahoma 74104
Novartis Investigator Site Austin Texas 78704
Novartis Investigator Site Carrollton Texas 75007
Novartis Investigator Site Dallas Texas 75246
Novartis Investigator Site Fort Worth Texas 75246
Novartis Investigator Site Mesquite Texas 75150
Novartis Investigator Site Arlington Virginia 22205
Novartis Investigator Site 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.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 31 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00554606, 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 Jul 8, 2021 · Synced Sep 4, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00554606 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →