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Completed Phase 2 Interventional

A Study of the Safety and Efficacy of ONO-4641 in Patients With Relapsing-Remitting Multiple Sclerosis

ClinicalTrials.gov ID: NCT01081782

Public ClinicalTrials.gov record NCT01081782. 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 Sep 6, 2026, 12:16 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 Double-Blind, Placebo-Controlled Study of the Safety and Efficacy of ONO-4641 in Patients With Relapsing-Remitting Multiple Sclerosis

Brief summary

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

The objective of this study is to evaluate the safety and efficacy of ONO-4641 in patients with relapsing-remitting multiple sclerosis over a 26-week treatment period.

Study identification

NCT ID
NCT01081782
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Ono Pharma USA Inc
Industry
Enrollment
407 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
Feb 28, 2010
Primary completion
Nov 30, 2011
Completion
Nov 30, 2011
Last update posted
Dec 24, 2013

2010 – 2011

United States locations

U.S. sites
23
U.S. states
16
U.S. cities
22
Facility City State ZIP Site status
Tucson Clinical Site 133 Tucson Arizona 85741
Aurora Clinical Site 132 Aurora Colorado 80045
Fort Collins Clinical Site 123 Fort Collins Colorado 80528
Fairfield Clinical Site 110 Fairfield Connecticut 06824
Ormond Beach Clinical Site 129 Ormond Beach Florida 32174
Sarasota Clinical Site 116 Sarasota Florida 34243
Sarasota Clinical Site 117 Sarasota Florida 34243
Northbrook Clinical Site 135 Northbrook Illinois 60062
Fort Wayne Clinical Site 111 Fort Wayne Indiana 46805
Indianapolis Clinical Site 121 Indianapolis Indiana 46202
Detroit Clinical Site 104 Detroit Michigan 48202
Farmington Hills Clinical Site 126 Farmington Hills Michigan 48334
Lebanon Clinical Site 115 Lebanon New Hampshire 03756
Albuquerque Clinical Site 106 Albuquerque New Mexico 87131
Rochester Clinical Site 108 Rochester New York 14642
Charlotte Clinical Site 125 Charlotte North Carolina 28204
HighPoint Clinical Site 128 HighPoint North Carolina 27265
Raleigh Clinical Site 103 Raleigh North Carolina 27607
Akron Clinical Site 112 Akron Ohio 44320
Philadelphia Clinical Site 120 Philadelphia Pennsylvania 19104
Knoxville Clinical Site 134 Knoxville Tennessee 37934
Round Rock Clinical Site 107 Round Rock Texas 78681
Seattle Clinical Site 118 Seattle Washington 98101

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 63 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01081782, 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 Dec 24, 2013 · Synced Sep 6, 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 protocol, eligibility criteria, and contact information for NCT01081782 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →