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Deferasirox

Generic Name
Deferasirox
Brand Names
Exjade, Jadenu, 恩瑞格, Deferasirox Accord, Deferasirox Mylan
Drug Type
Small Molecule
Chemical Formula
C21H15N3O4
CAS Number
201530-41-8
Unique Ingredient Identifier
V8G4MOF2V9
Background

Deferasirox is an iron chelator and the first oral medication FDA approved for chronic iron overload in patients receiving long term blood transfusions.

Indication

For the treatment of chronic iron overload due to blood transfusions (transfusional hemosiderosis) in patients 2 years of age and older.

Associated Conditions
Chronic Iron Overload
Associated Therapies
-

Observation of Patients With Transfusional Hemosiderosis Treatment With Deferasirox

Completed
Conditions
Transfusional Hemosiderosis
Interventions
First Posted Date
2011-07-14
Last Posted Date
2016-02-02
Lead Sponsor
Novartis Pharmaceuticals
Target Recruit Count
120
Registration Number
NCT01394029
Locations
🇬🇧

Novartis Investigative Site, London, United Kingdom

Effects of Iron Loading and Iron Chelation Therapy on Innate Immunity During Human Endotoxemia

Not Applicable
Completed
Conditions
Anemia
Systemic Inflammatory Process
Interventions
Drug: iron sucrose
Drug: Deferasirox
Drug: endotoxin
Drug: Placebo
First Posted Date
2011-05-06
Last Posted Date
2015-11-17
Lead Sponsor
Radboud University Medical Center
Target Recruit Count
30
Registration Number
NCT01349699

Open-Label Single-Arm Pilot Study in Adult Allogeneic Hematopoietic Stem Cell Transplant Recipients With Transfusional Iron Overload

Phase 4
Completed
Conditions
Iron Overload
Interventions
First Posted Date
2011-04-13
Last Posted Date
2012-05-01
Lead Sponsor
Novartis Pharmaceuticals
Target Recruit Count
30
Registration Number
NCT01335035
Locations
🇪🇸

Novartis Investigative Site, Murcia, Spain

Myelodysplastic Syndrome (MDS) Gastrointestinal (GI) Tolerability Study

Phase 4
Terminated
Conditions
Myelodysplastic Syndrome
Transfusional Iron Overload
Interventions
First Posted Date
2011-03-31
Last Posted Date
2017-03-03
Lead Sponsor
Novartis Pharmaceuticals
Target Recruit Count
12
Registration Number
NCT01326845
Locations
🇪🇸

Novartis Investigative Site, Madrid, Spain

Safety and Efficacy of Oral Deferasirox in Patients With Porphyria Cutanea Tarda

Phase 2
Conditions
Porphyria Cutanea Tarda
Interventions
First Posted Date
2011-01-27
Last Posted Date
2011-01-27
Lead Sponsor
Assistance Publique - Hôpitaux de Paris
Target Recruit Count
45
Registration Number
NCT01284946
Locations
🇫🇷

Hopital Louis Mourier, GI unit,, Colombes, Ile de France, France

Deferasirox in Treating Iron Overload Caused By Blood Transfusions in Patients With Hematologic Malignancies

Phase 2
Completed
Conditions
Adult Langerhans Cell Histiocytosis
Adult Acute Lymphoblastic Leukemia in Remission
Adult Acute Myeloid Leukemia With t(15;17)(q22;q12)
Adult Acute Myeloid Leukemia With t(8;21)(q22;q22)
Adult Grade III Lymphomatoid Granulomatosis
Angioimmunoblastic T-cell Lymphoma
Contiguous Stage II Adult Burkitt Lymphoma
Contiguous Stage II Adult Diffuse Large Cell Lymphoma
Contiguous Stage II Adult Diffuse Mixed Cell Lymphoma
Contiguous Stage II Adult Diffuse Small Cleaved Cell Lymphoma
Interventions
Drug: deferasirox
Other: laboratory biomarker analysis
Other: enzyme-linked immunosorbent assay
First Posted Date
2011-01-10
Last Posted Date
2018-09-07
Lead Sponsor
Wake Forest University Health Sciences
Target Recruit Count
16
Registration Number
NCT01273766
Locations
🇺🇸

Comprehensive Cancer Center of Wake Forest University, Winston-Salem, North Carolina, United States

This Study Will Evaluate Efficacy and Safety of Deferasirox in Patients With Myelodysplastic Syndromes (MDS), Thalassemia and Rare Anemia Types Having Transfusion-induced Iron Overload.

Phase 4
Completed
Conditions
Myelodysplastic Syndrome
Thalassemia
Interventions
First Posted Date
2010-12-01
Last Posted Date
2016-12-12
Lead Sponsor
Novartis Pharmaceuticals
Target Recruit Count
111
Registration Number
NCT01250951
Locations
🇷🇺

Novartis Investigative Site, St. Petersburg, Russian Federation

Deferasirox for Treating Patients Who Have Undergone Allogeneic Stem Cell Transplant and Have Iron Overload

Phase 2
Terminated
Conditions
Adult Acute Lymphoblastic Leukemia in Remission
Adult Acute Myeloid Leukemia in Remission
Adult Acute Myeloid Leukemia With Inv(16)(p13;q22)
Adult Acute Myeloid Leukemia With t(15;17)(q22;q12)
Atypical Chronic Myeloid Leukemia, BCR-ABL Negative
de Novo Myelodysplastic Syndromes
Iron Overload
Adult Acute Myeloid Leukemia With Del(5q)
Adult Acute Myeloid Leukemia With t(8;21)(q22;q22)
Chronic Eosinophilic Leukemia
Interventions
First Posted Date
2010-07-09
Last Posted Date
2019-06-18
Lead Sponsor
City of Hope Medical Center
Target Recruit Count
1
Registration Number
NCT01159067
Locations
🇺🇸

City of Hope, Duarte, California, United States

Safety and Efficacy of Deferasirox in Patients With Transfusion Dependent Iron Overload - a Non-comparative Extension Study

Phase 2
Completed
Conditions
Liver Iron Overload
Interventions
First Posted Date
2009-12-16
Last Posted Date
2011-08-11
Lead Sponsor
Novartis Pharmaceuticals
Target Recruit Count
70
Registration Number
NCT01033747
Locations
🇮🇹

Novartis Investigative Site, Torino, Italy

Clinical Importance of Treating Iron Overload in Sickle Cell Disease

Phase 3
Terminated
Conditions
Anemia, Sickle Cell
Transfusion Hemosiderosis
Interventions
First Posted Date
2009-09-22
Last Posted Date
2017-02-08
Lead Sponsor
Children's Hospital Los Angeles
Target Recruit Count
1
Registration Number
NCT00981370
Locations
🇺🇸

Childrens Hospital Los Angeles, Los Angeles, California, United States

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