Combination Deferasirox and Deferiprone for Severe Iron Overload in Thalassemia

Children's Hospital of Philadelphia (CHOP)

Status and phase

Completed

Phase 2

Phase 1

Conditions

Thalassemia Major With Severe Transfusional Iron Overload

Treatments

Drug: Deferasirox and deferiprone

Study type

Interventional

Funder types

Other

Identifiers

NCT01709032

12-009449

Details and patient eligibility

About

We hypothesize that the combination treatment with deferasirox and deferiprone will be well tolerated and will result in significant improvement in cardiac and liver iron levels.

Full description

Death and disability from iron related damage to the heart remain the most serious issue facing transfusion-dependent patients with thalassemia. However, over the past decade there have been several reports of improved survival and fewer cardiac complications. This improvement may be related to the availability of three chelators and also the accurate measurement of iron stores in various organs (e.g. heart and liver) with magnetic resonance imaging, which allows for personalized, tailored medical care for patients. The chelator characteristics, side effect profiles, and ability to remove iron from specific organs differ among the chelators, suggesting that combination therapy may be beneficial. Using two drugs at lower doses may be more tolerable than escalating doses of a single drug and may improve iron removal. The combination of deferoxamine and deferiprone has been shown to be particularly beneficial for reducing cardiac iron, but it requires a painful injection/infusion, which hinders adherence. This pilot study aims to investigate the safety of an oral-only combination chelator regimen (deferasirox and deferiprone) in individuals with thalassemia major with poorly controlled iron overload and to assess how well this chelator combination lowers iron stores over one year.

Enrollment

9 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

Alpha or beta thalassemia
Receiving chronic transfusions (at least 20 transfusions in lifetime) with iron overload requiring treatment with chelation
Serum ferritin >500 ng/ml
Liver iron concentration equal to or greater than 10 mg/g dw (by R2 MRI) or 7 to 10 mg/g dw (by R2 MRI) and not improving OR cardiac T2* between 6 and <20 ms
Women of childbearing age must have a negative pregnancy test
Agree to use approved method of contraception for the duration of the study
Subjects must have a good understanding of the study and be willing to comply with study procedures

Exclusion criteria

Subjects with past history of unexplained neutropenia (ANC < 1500/mcL), clinically significant renal disease (creatinine above the upper limit of normal), proteinuria >300 mg/L, clinically significant liver disease (ALT > 5x upper limit of normal), pulmonary or cardiovascular disease
History of other clinically relevant oral, endocrine, neurologic, psychiatric, immunologic, bone marrow or skin disorder that contraindicates dosing with deferasirox or deferiprone
History of adverse reaction or known allergy to either deferasirox or deferiprone necessitating drug discontinuation
Currently receiving treatment for active hepatitis
Use of any investigational agent in the past 30 days
Cardiac T2* <6 ms, left ventricular ejection fraction < 56%, and/or arrhythmia (certain subjects may be eligible if they have already had a trial of deferoxamine and deferiprone). Subjects who refuse to use deferoxamine after extensive consultation with at least 2 health care providers will also be allowed to participate.
Pregnant or breastfeeding females
Unwilling or unable to comply with study related procedures