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Completed Phase 3 Interventional Results available

To Evaluate Sarilumab - SAR153191 (REGN88) - Auto-injector Device In Patients With Rheumatoid Arthritis

ClinicalTrials.gov ID: NCT02057250

Public ClinicalTrials.gov record NCT02057250. 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 Oct 17, 2026, 3:20 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, Randomized, Open-Label, Parallel-Group Usability Study Of The Sarilumab Auto-Injector Device And A Prefilled Syringe In Patients With Moderate To Severe Active Rheumatoid Arthritis Who Are Candidates For Anti-IL6R Therapy

Brief summary

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

Primary Objective: To collect real-use data of the sarilumab auto-injector device (AID) used by rheumatoid arthritis (RA) participants. Secondary Objective: To compare the pharmacokinetic (PK) exposure of sarilumab administered by AID versus prefilled syringes (PFS).

Study identification

NCT ID
NCT02057250
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Sanofi
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
Mar 2014 (Type not available)
Primary completion
Feb 2015 (Actual)
Completion
Mar 2016 (Actual)
Last update posted
Jun 20, 2017

2014 – 2016

United States locations

U.S. sites
31
U.S. states
16
U.S. cities
28
Facility City State ZIP Site status
Investigational Site Number 840152 Huntsville Alabama 35801 —
Investigational Site Number 840221 Peoria Arizona 85381 —
Investigational Site Number 840226 Roseville California 95661 —
Investigational Site Number 840223 Boulder Colorado 80304 —
Investigational Site Number 840229 Miami Florida 33185 —
Investigational Site Number 840236 Orlando Florida 32804 —
Investigational Site Number 840155 Palm Harbor Florida 34684 —
Investigational Site Number 840220 South Miami Florida 33143 —
Investigational Site Number 840202 Hagerstown Maryland 21740 —
Investigational Site Number 840232 Flint Michigan 48504 —
Investigational Site Number 840233 Kalamazoo Michigan 49048 —
Investigational Site Number 840037 Tupelo Mississippi 38801 —
Investigational Site Number 840112 Lincoln Nebraska 68516 —
Investigational Site Number 840039 Albany New York 12208 —
Investigational Site Number 840224 Cincinnati Ohio 45219 —
Investigational Site Number 840002 Oklahoma City Oklahoma 73103 —
Investigational Site Number 840065 Tulsa Oklahoma 74135 —
Investigational Site Number 840009 Duncansville Pennsylvania 16635 —
Investigational Site Number 840062 Reading Pennsylvania 19611 —
Investigational Site Number 840016 North Charleston South Carolina 29406 —
Investigational Site Number 840025 Jackson Tennessee 38305 —
Investigational Site Number 840038 Austin Texas 78705 —
Investigational Site Number 840230 Carrollton Texas 75007 —
Investigational Site Number 840001 Dallas Texas 75231 —
Investigational Site Number 840020 Houston Texas 77034 —
Investigational Site Number 840239 Houston Texas 77034 —
Investigational Site Number 840241 Houston Texas 77034 —
Investigational Site Number 840242 Houston Texas 77034 —
Investigational Site Number 840069 Lubbock Texas 79424 —
Investigational Site Number 840074 Mesquite Texas 75150 —
Investigational Site Number 840237 Plano Texas 75042 —

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 22 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT02057250, 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 Jun 20, 2017 · Synced Oct 17, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT02057250 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →