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Completed Phase 3 Interventional

Efficacy and Safety of Arbaclofen Placarbil in Subjects With Spasticity Due to Multiple Sclerosis

ClinicalTrials.gov ID: NCT01359566

Public ClinicalTrials.gov record NCT01359566. 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, 1:19 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 Randomized, Double Blind, Placebo-Controlled Efficacy and Safety Study of Arbaclofen Placarbil in Subjects With Spasticity Due to Multiple Sclerosis

Brief summary

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

To evaluate the efficacy of three doses of XP19986 (arbaclofen placarbil) compared to placebo for the treatment of spasticity in subjects with multiple sclerosis (MS).

Study identification

NCT ID
NCT01359566
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
XenoPort, Inc.
Industry
Enrollment
228 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years to 70 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
May 2011 (Type not available)
Primary completion
Feb 2013 (Actual)
Completion
Feb 2013 (Actual)
Last update posted
Feb 21, 2021

2011 – 2013

United States locations

U.S. sites
28
U.S. states
18
U.S. cities
28
Facility City State ZIP Site status
XenoPort Clinical Site Phoenix Arizona 85004 —
XenoPort Clinical Site Tucson Arizona 85701 —
XenoPort Clinical Site Berkeley California 94705 —
XenoPort Clinical Site San Diego California 92103 —
XenoPort Clinical Site Denver Colorado 80012 —
XenoPort Clinical Site Port Charlotte Florida 33948 —
XenoPort Clinical Site Sarasota Florida 34231 —
XenoPort Clinical Site St. Petersburg Florida 33701 —
XenoPort Clinical Site Tampa Florida 33604 —
XenoPort Clinical Site Lake Barrington Illinois 60010 —
XenoPort Clinical Site Indianapolis Indiana 46204 —
XenoPort Clinical Site Lenexa Kansas 66210 —
XenoPort Clinical Site Lexington Kentucky 40505 —
XenoPort Clinical Site Bingham Farms Michigan 48025 —
XenoPort Clinical Site Detroit Michigan 48202 —
XenoPort Clinical Site Toms River New Jersey 08753 —
XenoPort Clinical Site Albuquerque New Mexico 87102 —
XenoPort Clinical Site Albany New York 12208 —
XenoPort Clinical Site Patchogue New York 11772 —
XenoPort Clinical Site Plainview New York 11803 —
XenoPort Clinical Site Asheville North Carolina 28805 —
XenoPort Clinical Site Akron Ohio 44320 —
XenoPort Clinical Site Franklin Tennessee 37064 —
XenoPort Clinical Site Nashville Tennessee 37205 —
XenoPort Clinical Site San Antonio Texas 78206 —
XenoPort Clinical Site Vienna Virginia 22181 —
XenoPort Clinical Site Seattle Washington 98108 —
XenoPort Clinical Site Tacoma Washington 98404 —

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 NCT01359566, 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 Feb 21, 2021 · 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 NCT01359566 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →