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Completed Phase 2 Interventional Results available

Study of Deferasirox for Treatment of Transfusional Iron Overload in Myelodysplastic Patients

ClinicalTrials.gov ID: NCT00110266

Public ClinicalTrials.gov record NCT00110266. 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 20, 2026, 9:44 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

An Open Label, Safety and Tolerability Study of Deferasirox for Treatment of Transfusional Iron Overload in Low-risk and INT-1, Myelodysplastic Patients Using Serum Ferritin Monitoring

Brief summary

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

The purpose of this trial is to examine the safety and efficacy of deferasirox in patients with Myelodysplastic Syndrome (MDS) and chronic iron overload from blood transfusions.

Study identification

NCT ID
NCT00110266
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Novartis Pharmaceuticals
Industry
Enrollment
176 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years and older
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 25, 2005 (Actual)
Primary completion
Mar 28, 2008 (Actual)
Completion
Mar 28, 2008 (Actual)
Last update posted
Aug 16, 2021

2005 – 2008

United States locations

U.S. sites
42
U.S. states
31
U.S. cities
39
Facility City State ZIP Site status
Univ of Alabama Birmingham Birmingham Alabama 35294 —
Mayo Clinic Phoenix Arizona 85054 —
Bay Area Cancer Research Group Concord California 94520 —
City of Hope National Medical Center Duarte California 91010 —
Cedars-Sinai Medical Center, UCLA School of Medicine Cedars-Sinai Medical Center Los Angeles California 90048 —
UCLA Medical Center Los Angeles California 90095-1678 —
UCSF San Francisco California 94143-0324 —
UCSF San Francisco California 94143 —
Rocky Mountain Cancer Centers Aurora Colorado 80012 —
Mayo Clinic Jacksonville Florida 32224 —
Emory University School of Medicine/Winship Cancer Institute Atlanta Georgia 30322 —
Straub Clinic and Hospital Honolulu Hawaii 96813 —
Novartis Investigative Site Chicago Illinois 60612 —
University of Chicago Hospital Chicago Illinois 60637-1470 —
University of Kansas Medical Center Kansas City Kansas 66160 —
University of Kentucky College of Medicine, Markey Cancer Center Lexington Kentucky 40536-0093 —
Cabrini Center for Cancer Care/Christus St. Frances Cabrini Hospital Alexandria Louisiana 71301 —
St. Agnes HealthCare Baltimore Maryland 21231-1000 —
Rush Cancer Institute Univ. of Massachussets Medical Center Worcester Massachusetts 01605 —
Novartis Investigative Site Southfield Michigan 48075 —
Mayo Clinic Rochester Minnesota 55905 —
The Center for Cancer Care & Research (TCCCR) St Louis Missouri 63110 —
Oncology Hematology West, PC Omaha Nebraska 68124-2346 —
Dartmouth Hitchcock Medical Center Lebanon New Hampshire 03756-0001 —
The Cancer Center at Hackensack University Hackensack New Jersey 07601 —
NMOHC Albuquerque New Mexico 87109 —
Roswell Park Cancer Center Buffalo New York 14623 —
Rochester General Hospital/Lipson Cancer and Blood Center Rochester New York 14621 —
Cancer Care of WNC Asheville North Carolina 28801 —
Wake Forest UniversitComprehensive Cancer Center Winston-Salem North Carolina 27157-1082 —
The Cleveland Clinic Foundation Cleveland Ohio 44195 —
The Ohio State University Columbus Ohio 43210 —
Novartis Investigative Site Portland Oregon 97239 —
Thomas Jefferson University; Jefferson Medical College, Kimmel Cancer Center Philadelphia Pennsylvania 19107 —
Western Pennsylvania Hospital Cancer Institute Pittsburgh Pennsylvania 15224 —
The West Cancer Clinic Memphis Tennessee 38120 —
Novartis Investigative site Nashville Tennessee 37232 —
Baylor/The Methodist Hospital Houston Texas 77030 —
Utah Cancer Specialists Salt Lake City Utah 84106 —
Arlington Fairfax Hematology Oncology PC Arlington Virginia 22205 —
Novartis Investigative Site Spokane Washington 99202 —
Medical College of Wisconsin 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.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 6 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00110266, 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 16, 2021 · Synced Oct 20, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00110266 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →