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Completed Phase 4 Interventional Results available

Study to Assess the Immunogenicity and Safety of Etanercept Produced Using a Modified Process in Patients With Plaque Psoriasis

ClinicalTrials.gov ID: NCT02274792

Public ClinicalTrials.gov record NCT02274792. 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 21, 2026, 1:45 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

A Single-arm Study to Assess the Immunogenicity and Safety of Etanercept Produced Using a Modified Process in Subjects With Plaque Psoriasis

Study identification

NCT ID
NCT02274792
Recruitment status
Completed
Study type
Interventional
Phase
Phase 4
Lead sponsor
Amgen
Industry
Enrollment
132 participants

Conditions and interventions

Interventions

  • Etanercept Drug

Drug

Eligibility (public fields only)

Age range
18 Years to 125 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
Dec 31, 2014
Primary completion
Oct 31, 2015
Completion
Oct 31, 2015
Last update posted
Dec 28, 2016

2015

United States locations

U.S. sites
33
U.S. states
18
U.S. cities
29
Facility City State ZIP Site status
Research Site Mobile Alabama 36608
Research Site Bakersfield California 93309
Research Site Beverly Hills California 90212
Research Site Fremont California 94538
Research Site Los Angeles California 90036
Research Site Denver Colorado 80210
Research Site Denver Colorado 80220
Research Site Aventura Florida 33180
Research Site Miami Florida 33144
Research Site Pembroke Pines Florida 33028
Research Site Carmel Indiana 46032
Research Site Indianapolis Indiana 46256
Research Site New Albany Indiana 47150
Research Site Overland Park Kansas 66202
Research Site Overland Park Kansas 66215
Research Site Louisville Kentucky 40202
Research Site Owensboro Kentucky 42303
Research Site Rockville Maryland 20850
Research Site Andover Massachusetts 01810
Research Site Worcester Massachusetts 01605
Research Site Clarkston Michigan 48346
Research Site Omaha Nebraska 68144
Research Site Verona New Jersey 07044
Research Site Raleigh North Carolina 27612
Research Site Cincinnati Ohio 45249
Research Site Johnston Rhode Island 02919
Research Site Nashville Tennessee 37205
Research Site Bellaire Texas 77401
Research Site Dallas Texas 75230
Research Site Dallas Texas 75231
Research Site San Antonio Texas 78229
Research Site San Antonio Texas 78249
Research Site Norfolk Virginia 23507

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 12 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT02274792, 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 28, 2016 · Synced Jul 21, 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 NCT02274792 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →