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Completed Phase 4 Interventional Results available

Rebif® Rebidose® Versus Rebiject II® Ease-of-Use

ClinicalTrials.gov ID: NCT02019550

Public ClinicalTrials.gov record NCT02019550. 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 21, 2026, 9:04 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 Phase IV, Randomized, Prospective, US-based, Multicenter, Cross-over Study Evaluating Subject Ease-of-use With Rebif® Rebidose® and Rebiject II® Autoinjectors in Subjects With Relapsing Remitting Multiple Sclerosis (RRMS) Treated With REBIF® 44 mcg Subcutaneously Three Times a Week

Brief summary

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

This is a Phase 4, prospective, open-label, randomized, cross-over, multicenter trial to evaluate ease-of-use with Rebif® Rebidose® and Rebiject II® autoinjectors in subjects with relapsing remitting multiple sclerosis (RRMS). Subjects will participate in the study for up to 10 weeks (including screening and treatment periods). The treatment period will last 8 weeks and include 12 self-injections using the Rebif® Rebidose® device and 12 self-injections using the Rebiject II® device.

Study identification

NCT ID
NCT02019550
Recruitment status
Completed
Study type
Interventional
Phase
Phase 4
Lead sponsor
EMD Serono
Industry
Enrollment
97 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years to 65 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
Mar 2014 (Type not available)
Primary completion
Jan 2016 (Actual)
Completion
Jan 2016 (Actual)
Last update posted
Mar 7, 2017

2014 – 2016

United States locations

U.S. sites
21
U.S. states
19
U.S. cities
21
Facility City State ZIP Site status
Research site Cullman Alabama 35058 —
Research Site Tuscon Arizona 85718 —
Research Site Newport Beach California 92663 —
Research site Fort Collins Colorado 80528 —
Research Site Dover Delaware 19901 —
Research Site Miami Florida 33136 —
Research site Sunrise Florida 33351 —
Research Site Atlanta Georgia 30327 —
Research Site Indianapolis Indiana 46256 —
Research site Foxborough Massachusetts 02035 —
Research site Golden Valley Minnesota 55422 —
Research Site Stratford New Jersey 08084 —
Research Site Patchogue New York 11772 —
Research Site Hickory North Carolina 28602 —
Research Site Winston-Salem North Carolina 27103 —
Research Site Dayton Ohio 45417 —
Research Site Oklahoma City Oklahoma 73104 —
Research Site Greensburg Pennsylvania 15601 —
Research site Spartanburg South Carolina 29307 —
Research Site Knoxville Tennessee 37934 —
Research site Mansfield Texas 76063 —

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 NCT02019550, 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 Mar 7, 2017 · Synced Oct 21, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT02019550 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →