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Terminated Phase 1 Interventional

A Safety and Efficacy Study of ELND002 in Patients With Relapsing Forms of Multiple Sclerosis

ClinicalTrials.gov ID: NCT01144351

Public ClinicalTrials.gov record NCT01144351. 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 26, 2026, 4:31 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 1b, Dose-Escalating, Randomized, Placebo-Controlled, Double-Blind Study to Evaluate the Safety and Efficacy of Subcutaneous ELND002 in Patients With Relapsing Forms of Multiple Sclerosis

Brief summary

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

The purpose of this study is to determine the safety and tolerability of ELND002 in patients with relapsing forms of secondary progressive multiple sclerosis (SPMS) or relapsing-remitting multiple sclerosis (RRMS).

Study identification

NCT ID
NCT01144351
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 1
Lead sponsor
Elan Pharmaceuticals
Industry
Enrollment
32 participants

Conditions and interventions

Interventions

Drug

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 2010 (Type not available)
Primary completion
Dec 2012 (Actual)
Completion
Not listed
Last update posted
Dec 14, 2015

Started 2010

United States locations

U.S. sites
17
U.S. states
12
U.S. cities
17
Facility City State ZIP Site status
Research Site Berkeley California 94705 —
Research Site Fresno California 93710 —
Research Site Newport Beach California 92663 —
Research Site Aurora Colorado 80045 —
Research Site Tampa Florida 33609 —
Research Site Vero Beach Florida 32960 —
Research Site Northbrook Illinois 60062 —
Research Site Farmington Hills Michigan 48334 —
Research Site Minneapolis Minnesota 55404 —
Research Site Albuquerque New Mexico 87106 —
Research Site Raleigh North Carolina 27607 —
Research Site Cincinnati Ohio 45219 —
Research Site Uniontown Ohio 44685 —
Research Site Cordova Tennessee 78258 —
Research Site Knoxville Tennessee 37920 —
Research Site San Antonio Texas 78258 —
Research Site Salt Lake City Utah 84106 —

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 3 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01144351, 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 14, 2015 · Synced Oct 26, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT01144351 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →