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Terminated Phase 3 Interventional Results available

This Was an Open-label, Single-arm Extension Study (CFTY720D2306E1) to a Double-blind, Randomized Multicenter, Placebo-controlled, Parallel-group Core Study (CFTY720D2306) in PPMS.

ClinicalTrials.gov ID: NCT00731692

Public ClinicalTrials.gov record NCT00731692. 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 Jul 22, 2026, 10:07 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, Randomized, Multicenter, Placebo-controlled, Parallel-group Study Comparing the Efficacy and Safety of 0.5mg Fingolimod Administered Orally Once Daily Versus Placebo in Patients With Primary Progressive Multiple Sclerosis and An Open-label, Single-arm Extension Study to the Double-blind, Randomized, Multicenter, Placebo-controlled, Parallel-group Study Comparing the Efficacy and Safety of0.5 mg FTY720 Administered Orally Once Daily Versus Placebo in Patients With Primary Progressive Multiple Sclerosis

Study identification

NCT ID
NCT00731692
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 3
Lead sponsor
Novartis Pharmaceuticals
Industry
Enrollment
970 participants

Conditions and interventions

Interventions

  • FTY720 Drug
  • Placebo Drug

Drug

Eligibility (public fields only)

Age range
25 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
Jul 27, 2008
Primary completion
Jun 21, 2015
Completion
Jun 21, 2015
Last update posted
Jun 13, 2017

2008 – 2015

United States locations

U.S. sites
33
U.S. states
21
U.S. cities
32
Facility City State ZIP Site status
Novartis Investigative Site Newport Beach California 92660
Novartis Investigative Site Sacramento California 95817
Novartis Investigative Site Aurora Colorado 80045
Novartis Investigative Site Pompano Beach Florida 33060
Novartis Investigative Site Tampa Florida 33609
Novartis Investigative Site Atlanta Georgia 30302
Novartis Investigative Site Chicago Illinois 60611
Novartis Investigative Site Chicago Illinois 60637
Novartis Investigative Site Kansas City Kansas 66160
Novartis Investigative Site Baltimore Maryland 21287
Novartis Investigative Site Boston Massachusetts 02135
Novartis Investigative Site Brookline Massachusetts 02445
Novartis Investigative Site Detroit Michigan 48201
Novartis Investigative Site St Louis Missouri 63110
Novartis Investigative Site Teaneck New Jersey 07666
Novartis Investigative Site Buffalo New York 14203
Novartis Investigative Site New York New York 10029
Novartis Investigative Site Rochester New York 14642
Novartis Investigative Site Stony Brook New York 11794
Novartis Investigative Site Charlotte North Carolina 28207
Novartis Investigative Site Durham North Carolina 27705
Novartis Investigative Site Cleveland Ohio 44195
Novartis Investigative Site Columbus Ohio 43221
Novartis Investigative Site Pittsburgh Pennsylvania 15213
Novartis Investigative Site Knoxville Tennessee 37934
Novartis Investigative Site Nashville Tennessee 37212
Novartis Investigative Site Dallas Texas 75390-9034
Novartis Investigative Site Houston Texas 77030
Novartis Investigative Site San Antonio Texas 78229
Novartis Investigative Site Burlington Vermont 05401
Novartis Investigative Site Charlottesville Virginia 22904
Novartis Investigative Site Seattle Washington 98122
Novartis Investigative Site Madison Wisconsin 53792

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 124 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00731692, 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 13, 2017 · Synced Jul 22, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00731692 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →