Efficacy and Safety of Deferasirox in Patients With Chronic Anemia and Transfusional Hemosiderosis

PHASE2CompletedINTERVENTIONAL
Enrollment

102

Participants

Timeline

Start Date

October 31, 2007

Primary Completion Date

January 31, 2011

Study Completion Date

February 29, 2012

Conditions
Chronic AnemiaTransfusional Hemosiderosis
Interventions
DRUG

Deferasirox (ICL670)

The recommended initial daily dose of Deferasirox is 20 mg/kg body weight.

Trial Locations (31)

34093

Novartis Investigative Site, Istanbul

35040

Novartis Investigative Site, Izmir

37007

Novartis Investigative Site, Salamanca

46026

Novartis Investigative Site, Valencia

169608

Novartis Investigative Site, Singapore

453-8511

Novartis Investigative Site, Nagoya

466-8560

Novartis Investigative Site, Nagoya

814-0180

Novartis Investigative Site, Fukuoka

060-8543

Novartis Investigative Site, Sapporo

663-8501

Novartis Investigative Site, Nishinomiya

920-0293

Novartis Investigative Site, Kahoku-gun

920-8641

Novartis Investigative Site, Kanazawa

589-8511

Novartis Investigative Site, Sayama

565-0871

Novartis Investigative Site, Suita

321-0293

Novartis Investigative Site, Shimotsuka-gun

329-0498

Novartis Investigative Site, Simotsuke-city

113-8655

Novartis Investigative Site, Bunkyo-ku

104-8560

Novartis Investigative Site, Cyuo-ku

108-8639

Novartis Investigative Site, Minato-ku

141-8625

Novartis Investigative Site, Shinagawa-ku

160-0023

Novartis Investigative Site, Shinjuku-ku

162-8666

Novartis Investigative Site, Shinjuku-ku

734-8551

Novartis Investigative Site, Hiroshima

860-0811

Novartis Investigative Site, Kumamoto

606-8507

Novartis Investigative Site, Kyoto

852-8501

Novartis Investigative Site, Nagasaki

930-8550

Novartis Investigative Site, Toyama

02-097

Novartis Investigative Site, Warsaw

02-776

Novartis Investigative Site, Warsaw

01330

Novartis Investigative Site, Adana

06100

Novartis Investigative Site, Ankara

Sponsors
All Listed Sponsors
lead

Novartis Pharmaceuticals

INDUSTRY