Combination Therapy Compared With Single-Drug Therapy in Patients With Cardiac Diseases
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ClinicalTrials.gov Identifier: NCT00115349 |
Recruitment Status :
Terminated
(due to low enrollment)
First Posted : June 22, 2005
Results First Posted : January 14, 2014
Last Update Posted : March 1, 2018
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Condition or disease | Intervention/treatment | Phase |
---|---|---|
Cardiovascular Diseases Heart Diseases Beta-Thalassemia | Drug: Deferoxamine Drug: Deferiprone (L1) | Phase 2 |
DESIGN NARRATIVE:
Participants will be randomized to 1 year of treatment with L1/DFO combination therapy or DFO monotherapy. At baseline, 6 months, and 1 year on therapy, cardiac function will be assessed by MRI measurement of left ventricular ejection fraction (LVEF), T2*, Holter monitoring, and electrocardiography. Additional monitoring for safety includes weekly blood testing, monthly visits, and periodic eye and ear exams.
Study Type : | Interventional (Clinical Trial) |
Actual Enrollment : | 20 participants |
Allocation: | Randomized |
Intervention Model: | Parallel Assignment |
Masking: | Triple (Participant, Care Provider, Investigator) |
Primary Purpose: | Treatment |
Official Title: | Thalassemia Clinical Research Network - Cardiac L1/DFO Trial |
Study Start Date : | June 2005 |
Actual Primary Completion Date : | July 2008 |
Actual Study Completion Date : | April 2009 |

Arm | Intervention/treatment |
---|---|
Experimental: L1/DFO
Deferoxamine (DFO) and deferiprone (L1) combination therapy
|
Drug: Deferoxamine
Deferoxamine will be given daily for 12-24h/day 7 days a week either subcutaneous or intravenous at up to 50-60 mg/kg/day.
Other Name: DFO Drug: Deferiprone (L1) The dose of L1, 75mg/kg in three divided oral doses, is the maximum dose at which toxicity has been tested in prospective trials
Other Name: L1 |
Active Comparator: DFO
Deferoxamine (DFO) monotherapy
|
Drug: Deferoxamine
Deferoxamine will be given daily for 12-24h/day 7 days a week either subcutaneous or intravenous at up to 50-60 mg/kg/day.
Other Name: DFO |
- Change in Left Ventricular Ejection Fraction (LVEF). [ Time Frame: Baseline to one year ]The primary outcome variable is change in left ventricular ejection fraction (blood ejected from the heart into the body) as measured by MRI from baseline to one year. The unit of primary outcome (left ventricular ejection fraction) is the percent of the blood in left ventricle.
- Evaluate Whether L1/DFO Combination Therapy is Superior to DFO Monotherapy in Lowering Myocardial Iron Burden Estimated by Myocardial T2*. [ Time Frame: one year ]
- Change in Left Ventricular (LV) Volume From Screening to One Year. [ Time Frame: one year ]
- Change in ECHO LV Volume, Ejection Fraction, Shortening Fraction, and VCFc/Wall Stress Z-score From Baseline to One Year. [ Time Frame: one year ]
- Change in Holter Monitor Scores From Baseline to One Year. [ Time Frame: one year ]
- Initiation of or Increase in Cardiac Medications [ Time Frame: continuous ]
- Adverse Events [ Time Frame: continous ]

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Ages Eligible for Study: | 18 Years to 100 Years (Adult, Older Adult) |
Sexes Eligible for Study: | All |
Accepts Healthy Volunteers: | No |
Inclusion Criteria:
- Transfusion-dependent beta-thalassemia (eight or more transfusion episodes in the previous year)
- Left ventricular ejection fraction by MRI less than or equal to 56% by balanced steady-state free precession (SSFP) or 63% by spoiled gradient recalled echo (SPGR)
- Currently on treatment with subcutaneous or intravenous DFO; participants must be willing and able to chelate 7 days per week 12 - 24 hours per day
- Serum ferritin greater than 1000 µg/L or ferritin between 500 µg/L and 1000 µg/L and cardiac T2* less than 20 ms
Exclusion Criteria:
- Pacemaker, severe claustrophobia, or other contraindications to MRI; severe congestive heart failure (New York Heart Association Classification IV); congenital or acquired valvular heart disease significant enough to require surgery or medications
- Currently receiving treatment for hepatitis; renal insufficiency defined by a clinically significant abnormal serum creatinine with a calculated creatinine clearance of less than 50 ml/min according to the Cockroft formula
- A neutrophil count less than 1.5 x 109/L on two or more occasions at least 4 weeks apart within the past year and not associated with an acute viral illness or a platelet count less than 80 x 109/L on two or more occasions at least 4 weeks apart within the past year
- Treatment with L1 or Exjade during the previous 2 weeks or previous adverse experience to L1 requiring suspension
- Infection with HIV
- Active participation in other investigational drug or device studies
- Unwilling to consider treatment with DFO at a dose of 50-60 mg/kg 12-24 hours per day 7 days per week
- Women who are pregnant or breast feeding
- Systemic infection or cardiovascular, hepatic, renal, pulmonary, or gastrointestinal disease that would prevent patients from undergoing any of the study-required treatments or procedures or requires treatment with any contraindicated medication(s)
- Presence of any other condition that, in the opinion of the investigator, would make the patient unsuitable for enrollment or could interfere with the patient's compliance with the protocol; may include but is not limited to alcohol or drug abuse
- For women of child-bearing potential, an inability or unwillingness to use a highly effective method of contraception (e.g., implants, injectables, combined oral contraceptives, or some intrauterine devices)

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT00115349
United States, California | |
Children's Hospital of Los Angeles | |
Los Angeles, California, United States, 90027 | |
Children's Hospital | |
Oakland, California, United States, 94609 | |
United States, Illinois | |
Children's Memorial Hospital | |
Chicago, Illinois, United States, 60614-3394 | |
United States, Massachusetts | |
Children's Hospital | |
Boston, Massachusetts, United States, 02115 | |
United States, New York | |
Weill Medical College of Cornell University | |
New York, New York, United States, 10021 | |
United States, Pennsylvania | |
Children's Hospital of Philadelphia | |
Philadelphia, Pennsylvania, United States, 19104-4399 |
Principal Investigator: | John Porter, MD | University College, London | |
Study Chair: | Patricia J. Giardina, MD | Weill Medical College of Cornell University | |
Study Chair: | Ellis J. Neufeld, MD | Boston Children's Hospital | |
Study Chair: | Elliott P, Vichinsky, MD | Children's Hospital and Research Institute, Oakland | |
Study Chair: | Sonja McKinlay, Ph.D. | New England Research Institutes, Inc. |
Responsible Party: | HealthCore-NERI |
ClinicalTrials.gov Identifier: | NCT00115349 |
Other Study ID Numbers: |
181 U01HL065260 ( U.S. NIH Grant/Contract ) U01HL065244 ( U.S. NIH Grant/Contract ) U01HL065239 ( U.S. NIH Grant/Contract ) U01HL065238 ( U.S. NIH Grant/Contract ) U01HL065232 ( U.S. NIH Grant/Contract ) |
First Posted: | June 22, 2005 Key Record Dates |
Results First Posted: | January 14, 2014 |
Last Update Posted: | March 1, 2018 |
Last Verified: | January 2014 |
Cardiovascular Diseases Heart Diseases Thalassemia beta-Thalassemia Anemia, Hemolytic, Congenital Anemia, Hemolytic Anemia Hematologic Diseases Hemoglobinopathies |
Genetic Diseases, Inborn Deferiprone Deferoxamine Iron Chelating Agents Chelating Agents Sequestering Agents Molecular Mechanisms of Pharmacological Action Siderophores |