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Completed Phase 4 Interventional Results available

Preference Between Two Autoinjectors in Patients With Rheumatoid Arthritis and Plaque Psoriasis Treated With Etanercept

ClinicalTrials.gov ID: NCT01875991

Public ClinicalTrials.gov record NCT01875991. 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 2, 2026, 5:44 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, Randomized, Crossover Study to Assess the Preference for Autoinjector A Versus Autoinjector B in Rheumatoid Arthritis and Plaque Psoriasis Subjects Treated With Etanercept

Brief summary

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

The study will estimate the preference of rheumatoid arthritis (RA) and Plaque Psoriasis (PsO) patients who self inject etanercept for one of two experimental autoinjectors.

Study identification

NCT ID
NCT01875991
Recruitment status
Completed
Study type
Interventional
Phase
Phase 4
Lead sponsor
Amgen
Industry
Enrollment
217 participants

Conditions and interventions

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
Jun 4, 2013
Primary completion
Mar 3, 2014
Completion
Mar 3, 2014
Last update posted
Sep 3, 2018

2013 – 2014

United States locations

U.S. sites
28
U.S. states
20
U.S. cities
28
Facility City State ZIP Site status
Research Site Huntsville Alabama 35801
Research Site Tuscaloosa Alabama 35406
Research Site Glendale Arizona 85304
Research Site Scottsdale Arizona 85258
Research Site Hot Springs Arkansas 71913
Research Site San Diego California 92108
Research Site San Ramon California 94583
Research Site Santa Maria California 93454-6945
Research Site Tustin California 92780
Research Site Denver Colorado 80230
Research Site Dunedin Florida 34698
Research Site Tampa Florida 33614
Research Site Overland Park Kansas 66215
Research Site Louisville Kentucky 40217
Research Site Frederick Maryland 21702
Research Site Lansing Michigan 48910
Research Site Lincoln Nebraska 68516
Research Site Orchard Park New York 14127
Research Site Bismarck North Dakota 58502
Research Site Dayton Ohio 45417
Research Site Oklahoma City Oklahoma 73103
Research Site Duncansville Pennsylvania 16635
Research Site Wyomissing Pennsylvania 19610
Research Site Charleston South Carolina 29414
Research Site Hixson Tennessee 37343
Research Site Austin Texas 78731
Research Site Dallas Texas 75231
Research Site Clarksburg West Virginia 26301

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 9 non-U.S. sites.

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About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01875991, 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 Sep 3, 2018 · Synced Sep 2, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT01875991 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →