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Completed Phase 3 Interventional Results available

A Multi-Site, Open-Label Extension Trial of Oral RPC1063 in Relapsing Multiple Sclerosis

ClinicalTrials.gov ID: NCT02576717

Public ClinicalTrials.gov record NCT02576717. 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 19, 2026, 4:26 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 Phase 3, Multi-Center, Randomized, Double-Blind, Double-Dummy, Active Controlled, Parallel Group Study To Evaluate The Efficacy And Safety Of RPC1063 Administered Orally To Relapsing Multiple Sclerosis Patients

Brief summary

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

The purpose of the trial is to determine the safety and efficacy of RPC1063 in patients with relapsing multiple sclerosis.

Study identification

NCT ID
NCT02576717
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Celgene
Industry
Enrollment
2,494 participants

Conditions and interventions

Interventions

Drug

Eligibility (public fields only)

Age range
18 Years to 55 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
Oct 16, 2015 (Actual)
Primary completion
Jan 5, 2023 (Actual)
Completion
Jan 5, 2023 (Actual)
Last update posted
Jan 30, 2024

2015 – 2023

United States locations

U.S. sites
19
U.S. states
10
U.S. cities
18
Facility City State ZIP Site status
Local Institution - 115 Phoenix Arizona 85004 —
Local Institution - 118 Phoenix Arizona 85013 —
Local Institution - 110 Berkeley California 94705 —
Local Institution - 103 Fresno California 93710 —
Local Institution - 122 Long Beach California 90806 —
Local Institution - 112 Sacramento California 95817 —
Local Institution - 120 San Francisco California 94158 —
Local Institution - 114 Maitland Florida 32751 —
Local Institution - 123 Port Charlotte Florida 33952 —
Local Institution - 124 Sunrise Florida 33351 —
Local Institution - 147 Tampa Florida 33609 —
Local Institution - 137 Golden Valley Minnesota 55422 —
Local Institution - 170 Las Vegas Nevada 89106 —
Local Institution - 143 Raleigh North Carolina 27607 —
Local Institution - 107 Westerville Ohio 43801 —
Local Institution - 144 Knoxville Tennessee 37922 —
Local Institution - 138 Lubbock Texas 79410 —
Local Institution - 179 Round Rock Texas 78681 —
Local Institution - 141 Kirkland Washington 98034 —

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 156 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT02576717, 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 Jan 30, 2024 · Synced Oct 19, 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 public registry record, listed eligibility criteria, and available contact information for NCT02576717 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →