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Completed Phase 3 Interventional

Efficacy and Safety of FTY720 in Patients Who Receive a Kidney Transplant

ClinicalTrials.gov ID: NCT00099736

Public ClinicalTrials.gov record NCT00099736. 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 3, 2026, 8:34 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Brief summary

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

The efficacy and safety of FTY720 is being evaluated in patients who receive a kidney transplant.

Study identification

NCT ID
NCT00099736
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Novartis Pharmaceuticals
Industry
Enrollment
696 participants

Conditions and interventions

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
May 6, 2003
Primary completion
Sep 18, 2005
Completion
Sep 18, 2005
Last update posted
Aug 21, 2017

2003 – 2005

United States locations

U.S. sites
42
U.S. states
26
U.S. cities
39
Facility City State ZIP Site status
Not listed Phoenix Arizona 85054
Not listed Los Angeles California 90057
Not listed Palo Alto California 94303
Not listed San Francisco California 94143
Not listed Denver Colorado 80262
Not listed New Haven Connecticut 06520
Not listed Tampa Florida 33606
Not listed Atlanta Georgia 30309
Not listed Atlanta Georgia 30322
Not listed Augusta Georgia 30912
Not listed Chicago Illinois 60612
Not listed Indianapolis Indiana 46202
Not listed Des Moines Iowa 50309
Not listed Portland Maine 04102
Not listed Boston Massachusetts 02111
Not listed Boston Massachusetts 02215
Not listed Ann Arbor Michigan 48109
Not listed Detroit Michigan 48202
Not listed Minneapolis Minnesota 55455
Not listed Rochester Minnesota 55905
Not listed Omaha Nebraska 68198
Not listed Livingston New Jersey 07039
Not listed Hawthorne New York 10523
Not listed Chapel Hill North Carolina 27599
Not listed Durham North Carolina 27710
Not listed Cleveland Ohio 44106
Not listed Cleveland Ohio 44195
Not listed Toledo Ohio 43614
Not listed Portland Oregon 97232
Not listed Philadelphia Pennsylvania 19102
Not listed Charleston South Carolina 29425
Not listed Memphis Tennessee 38103
Not listed Nashville Tennessee 37212
Not listed Dallas Texas 75246
Not listed Galveston Texas 77555
Not listed Houston Texas 77030
Not listed San Antonio Texas 78229
Not listed Salt Lake City Utah 84132
Not listed Fairfax Virginia 22042
Not listed Richmond Virginia 23298
Not listed Madison Wisconsin 53792
Not listed Milwaukee Wisconsin 53226

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 NCT00099736, 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 Aug 21, 2017 · Synced Sep 3, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00099736 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →