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Completed Phase 2 Interventional Results available

A Combination Trial of Copaxone Plus Estriol in Relapsing Remitting Multiple Sclerosis (RRMS)

ClinicalTrials.gov ID: NCT00451204

Public ClinicalTrials.gov record NCT00451204. 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 18, 2026, 8:30 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 Combination Trial of Copaxone Plus Estriol in RRMS

Brief summary

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

This is a double-blinded, placebo controlled study of estriol pills versus placebo pills in relapsing remitting multiple sclerosis. The study treatment will be an added on to Copaxone injections in all subjects. The primary outcome measure is a reduction in relapses.

Study identification

NCT ID
NCT00451204
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Enrollment
158 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years to 50 Years
Sex
Female
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 2007 (Type not available)
Primary completion
Jul 2014 (Actual)
Completion
Jul 2014 (Actual)
Last update posted
Jun 16, 2016

2007 – 2014

United States locations

U.S. sites
15
U.S. states
15
U.S. cities
15
Facility City State ZIP Site status
Mayo Clinic Scottsdale Arizona 85259 —
University of California, Los Angeles Los Angeles California 90095 —
University of Colorado Aurora Colorado 80045 —
University of Chicago Chicago Illinois 60637 —
University of Kansas Kansas City Kansas 66160 —
Johns Hopkins University Baltimore Maryland 21287-6965 —
University of Minnesota Minneapolis Minnesota 55455 —
Washington University St Louis Missouri 63110 —
Dartmouth Medical School Lebanon New Hampshire 03765 —
UMDNJ-Robert Wood Johnson Medical Center New Brunswick New Jersey 08901 —
University of New Mexico Albuquerque New Mexico 87131 —
Ohio State University Columbus Ohio 43221 —
University of Pennsylvania Philadelphia Pennsylvania 19104 —
University of Texas Southwestern Dallas Texas 75390-8575 —
Western Institute for Biomedical Research Salt Lake City Utah 84158 —

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 1 non-U.S. site.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00451204, 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 Jun 16, 2016 · Synced Oct 18, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00451204 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →