Safety and Efficacy of Deferasirox (ICL670) in Patients With Iron Overload Resulting From Hereditary Hemochromatosis

PHASE1/PHASE2CompletedINTERVENTIONAL
Enrollment

49

Participants

Timeline

Start Date

August 31, 2006

Primary Completion Date

December 31, 2007

Study Completion Date

March 31, 2009

Conditions
Iron OverloadHereditary Hemochromatosis
Interventions
DRUG

Deferasirox (ICL670)

Trial Locations (18)

14625

Rochester General Hospital, Rochester

28203

Carolinas Medical Center, Charlotte

29203

Three Medical Park, Columbia

43210

Ohio State University Medical Center, Columbus

48202

Henry Ford Health System, Detroit

55905

Mayo Clinic, Rochester

63110

St. Louis University, St Louis

90822

UC Irvine/Long Beach, Long Beach

06030

University of Connecticut Health Center, Farmington

Unknown

Novartis Investigative Site, Brisbane

Novartis Investigative Site, London

Novartis Investigative Site, Rennes

Novartis Investigative Site, Chemnitz

Novartis Investigative Site, Heidelberg

Novartis Investigative Site, Magdeburg

Novartis Investigative Site, Oberhausen

Novartis Investigative Site, Modena

Novartis Investigative Site, Monza

Sponsors
All Listed Sponsors
lead

Novartis Pharmaceuticals

INDUSTRY