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Deferasirox

Alternative Names: deferasirox, exjade, icl 670, icl670, dst-0509, jadenu, deferasorox
Latest Update: 2025-01-20
Latest Update Note: Clinical Trial Update

Product Description

Deferasirox is used to remove excess iron from the body in patients who have had too many blood transfusions and in patients with non-transfusion dependent thalassemia syndromes. Deferasirox is an iron chelator (binder). It combines with iron in the blood. The combination of iron and deferasirox is then removed from the body by the kidneys. If you have too much iron in the body, it can damage various organs and tissues. (Sourced from: https://www.mayoclinic.org/drugs-supplements/deferasirox-oral-route/side-effects/drg-20070776?p=1)

Mechanisms of Action: Iron Antagonist

Novel Mechanism: No

Modality: Small Molecule

Route of Administration: Oral

FDA Designation: None *

Approval Status: Approved

Approved Countries: Algeria | Argentina | Australia | Austria | Bangladesh | Belgium | Bosnia | Brazil | Bulgaria | Canada | Chile | Colombia | Croatia | Cyprus | Czech | Denmark | Dominican Republic | Ecuador | Egypt | Estonia | European Medicines Agency | Finland | France | Germany | Greece | Hong Kong | Hungary | Iceland | India | Indonesia | Ireland | Israel | Italy | Japan | Jordan | Korea | Latvia | Lebanon | Lithuania | Luxembourg | Malaysia | Malta | Mexico | Morocco | Netherlands | New Zealand | Norway | Pakistan | Peru | Philippines | Poland | Portugal | Romania | Russia | Saudi Arabia | Serbia | Singapore | Slovakia | Slovenia | South Africa | Spain | Sri Lanka | Sweden | Switzerland | Taiwan | Thailand | Tunisia | Turkey | Ukraine | United Arab Emirates | United Kingdom | United States | Uruguay | Venezuela | Vietnam

Approved Indications: Thalassemia | Iron Overload

Known Adverse Events: Abdominal Pain | Pain Unspecified | Transfusion Reaction | Iron Overload | Diarrhea

Company: Novartis
Company Location: BASEL V8 CH 4056
Company CEO: Vasant Narasimhan
Additonal Commercial Interests: None

Clinical Description

Map of Global Clinical Trials for Deferasirox

Countries in Clinic: France

Active Clinical Trial Count: 8

Highest Development Phases

Phase 2: Anemia, Sickle Cell|Hemochromatosis|Iron Overload|Myelodysplastic Syndrome|Preleukemia|beta-Thalassemia

Phase 1: Healthy Volunteers|Ranula

Trial

Phase

Trial Status

Disease

Primary Completion Date

Probability of Success

LODEFI

P2

Completed

Myelodysplastic Syndrome|Preleukemia

2024-10-01

2016-002529-12

P2

Active, not recruiting

Hemochromatosis

2020-11-16

2015-003532-12

P2

Active, not recruiting

beta-Thalassemia

2020-03-27

Study of Deferasirox Relative to Subcutaneous Deferoxamine in Sickle Cell Disease

P2

Active, not recruiting

Anemia, Sickle Cell|Iron Overload

2020-03-05

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