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Completed Phase 3 Interventional Results available

Study to Test the Safe and Effective Use of an e-Device for the Self-injection of Certolizumab Pegol Solution by Subjects With Moderate to Severe Active Rheumatoid Arthritis, Active Ankylosing Spondylitis, Active Psoriatic Arthritis, or Moderately to Severely Active Crohn's Disease

ClinicalTrials.gov ID: NCT03357471

Public ClinicalTrials.gov record NCT03357471. 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 18, 2026, 4:56 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 Multicenter, Open-Label Study to Evaluate the Safe and Effective Use of an Electro-Mechanical Injection Device (E-Device) for the Subcutaneous Self-Injection of Certolizumab Pegol Solution by Subjects With Moderate to Severe Active Rheumatoid Arthritis, Active Ankylosing Spondylitis, Active Psoriatic Arthritis, or Moderately to Severely Active Crohn's Disease

Study identification

NCT ID
NCT03357471
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
UCB Biopharma S.P.R.L.
Industry
Enrollment
70 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
Nov 2, 2017
Primary completion
Jul 1, 2018
Completion
Jul 1, 2018
Last update posted
Oct 24, 2019

2017 – 2018

United States locations

U.S. sites
22
U.S. states
12
U.S. cities
18
Facility City State ZIP Site status
Ra0098 116 Mesa Arizona 85202
Ra0098 107 Mesa Arizona 85306
Ra0098 135 Phoenix Arizona 85037
Ra0098 119 Tucson Arizona 85704
Ra0098 101 Covina California 91722
Ra0098 131 Clermont Florida 34711
Ra0098 132 Coral Springs Florida 33071
Ra0098 127 Gainesville Georgia 30501
Ra0098 122 Clive Iowa 50265
Ra0098 105 St Louis Missouri 63110
Ra0098 104 St Louis Missouri 63128
Ra0098 103 Dover New Jersey 07801
Ra0098 117 Great Neck New York 11021
Ra0098 113 Myrtle Beach South Carolina 29572
Ra0098 126 Hixson Tennessee 37343
Ra0098 111 Austin Texas 78731
Ra0098 123 Austin Texas 78745
Ra0098 102 Austin Texas 78758
Ra0098 128 Corpus Christi Texas 78404
Ra0098 106 Nassau Bay Texas 77058
Ra0098 114 San Antonio Texas 78229
Ra0098 133 Richland Washington 99352

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT03357471, 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 Oct 24, 2019 · Synced May 18, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT03357471 live on ClinicalTrials.gov.

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