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Completed Phase 2 Interventional

Study Evaluating Long-Term Safety Of ATN-103 In Subjects With Rheumatoid Arthritis

ClinicalTrials.gov ID: NCT01063803

Public ClinicalTrials.gov record NCT01063803. 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 8, 2026, 1:35 PM EDT

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

Official title

An Open-Label Extension Study To Assess The Long-term Safety And Tolerability Of ATN-103 In Subjects With Rheumatoid Arthritis

Brief summary

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

This open-label extension study will allow subjects who have completed either the 3242K1-2000-WW or 3242K1-2001-JA study to receive up to an additional 48 weeks of ATN-103 treatment and will provide data on the long-term safety and tolerability of ATN-103 in subjects with rheumatoid arthritis.

Study identification

NCT ID
NCT01063803
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Ablynx, a Sanofi company
Industry
Enrollment
266 participants

Conditions and interventions

Interventions

Drug

Eligibility (public fields only)

Age range
18 Years to 80 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
Jan 31, 2010
Primary completion
Jan 31, 2012
Completion
Jan 31, 2012
Last update posted
Apr 10, 2016

2010 – 2012

United States locations

U.S. sites
25
U.S. states
17
U.S. cities
25
Facility City State ZIP Site status
Investigational Site Birmingham Alabama 35216
Investigational Site Huntsville Alabama 35801
Investigational Site Peoria Arizona 85381
Investigational Site Riverside California 92501
Investigational Site Upland California 91786
Investigational Site Bridgeport Connecticut 06606
Investigational Site Newark Delaware 19713
Investigational Site Ocala Florida 34474
Investigational Site Port Orange Florida 32127
Investigational Site Vero Beach Florida 32960
Investigational Site Coeur d'Alene Idaho 83814
Investigational Site Frederick Maryland 21702
Investigational Site Lansing Michigan 48910
Investigational Site Freehold New Jersey 07728
Investigational Site Charlotte North Carolina 28210
Investigational Site Winston-Salem North Carolina 27157
Investigational Site Columbus Ohio 43213
Investigational Site Oklahoma City Oklahoma 73103
Investigational Site Tulsa Oklahoma 74104
Investigational Site Lake Oswego Oregon 97035
Investigational Site Columbia South Carolina 29204
Investigational Site Myrtle Beach South Carolina 29572
Investigational Site Nashville Tennessee 37205
Investigational Site Dallas Texas 75231
Investigational Site San Antonio Texas 78217

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 42 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01063803, 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 Apr 10, 2016 · Synced Sep 8, 2026

Related: full search, browse by condition, browse by drug or therapy, browse by sponsor, browse by U.S. city.

Open the official record

The complete protocol, eligibility criteria, and contact information for NCT01063803 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →