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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
Conditions
Interventions
e-Device
Locations
22
United States
Ra0098 116
Mesa, Arizona, United States
Ra0098 107
Mesa, Arizona, United States
Ra0098 135
Phoenix, Arizona, United States
Ra0098 119
Tucson, Arizona, United States
Ra0098 101
Covina, California, United States
Ra0098 131
Clermont, Florida, United States
Start Date
November 3, 2017
Primary Completion Date
July 2, 2018
Completion Date
July 2, 2018
Last Updated
October 25, 2019
NCT04314531
NCT05814939
Lead Sponsor
UCB Biopharma S.P.R.L.
Data Source & Attribution
This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.
Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.
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