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Completed Phase 3 Interventional Results available

Long-term Safety and Efficacy of ABP 501 in Subjects With Moderate to Severe Rheumatoid Arthritis

ClinicalTrials.gov ID: NCT02114931

Public ClinicalTrials.gov record NCT02114931. 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 May 6, 2026, 7:34 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, Single-arm Extension Study to Evaluate the Long-term Safety and Efficacy of ABP 501 in Subjects With Moderate to Severe Rheumatoid Arthritis

Study identification

NCT ID
NCT02114931
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Amgen
Industry
Enrollment
467 participants

Conditions and interventions

Interventions

  • ABP 501 Biological

Biological

Eligibility (public fields only)

Age range
18 Years to 81 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
Mar 31, 2014
Primary completion
Mar 31, 2016
Completion
Mar 31, 2016
Last update posted
Apr 23, 2017

2014 – 2016

United States locations

U.S. sites
29
U.S. states
17
U.S. cities
29
Facility City State ZIP Site status
Research Site Huntsville Alabama 35801
Research Site Peoria Arizona 85381
Research Site Scottsdale Arizona 85258
Research Site Covina California 91723
Research Site El Cajon California 92020
Research Site Hemet California 92543
Research Site Palm Desert California 92260
Research Site Van Nuys California 91405
Research Site Whittier California 90602
Research Site Danbury Connecticut 06810
Research Site Miami Florida 33015
Research Site Orlando Florida 32804
Research Site Sarasota Florida 34233
Research Site Sandy Springs Georgia 30328
Research Site Lexington Kentucky 40504
Research Site Hagerstown Maryland 21740
Research Site Wheaton Maryland 20902
Research Site St Louis Missouri 63141
Research Site Omaha Nebraska 68114
Research Site Brooklyn New York 11201
Research Site Mineola New York 11501
Research Site Oklahoma City Oklahoma 73103
Research Site Bethlehem Pennsylvania 18015
Research Site Duncansville Pennsylvania 16635
Research Site Charleston South Carolina 29406
Research Site Memphis Tennessee 38119
Research Site Carrollton Texas 75007
Research Site Dallas Texas 75231
Research 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 48 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT02114931, 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 23, 2017 · Synced May 6, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT02114931 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →