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Combination Therapy Compared With Single-Drug Therapy in Patients With Cardiac Diseases

Primary Purpose

Cardiovascular Diseases, Heart Diseases, Beta-Thalassemia

Status
Terminated
Phase
Phase 2
Locations
United States
Study Type
Interventional
Intervention
Deferoxamine
Deferiprone (L1)
Sponsored by
Carelon Research
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Cardiovascular Diseases

Eligibility Criteria

18 Years - 100 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

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)

Sites / Locations

  • Children's Hospital of Los Angeles
  • Children's Hospital
  • Children's Memorial Hospital
  • Children's Hospital
  • Weill Medical College of Cornell University
  • Children's Hospital of Philadelphia

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

L1/DFO

DFO

Arm Description

Deferoxamine (DFO) and deferiprone (L1) combination therapy

Deferoxamine (DFO) monotherapy

Outcomes

Primary Outcome Measures

Change in Left Ventricular Ejection Fraction (LVEF).
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.

Secondary Outcome Measures

Evaluate Whether L1/DFO Combination Therapy is Superior to DFO Monotherapy in Lowering Myocardial Iron Burden Estimated by Myocardial T2*.
Change in Left Ventricular (LV) Volume From Screening to One Year.
Change in ECHO LV Volume, Ejection Fraction, Shortening Fraction, and VCFc/Wall Stress Z-score From Baseline to One Year.
Change in Holter Monitor Scores From Baseline to One Year.
Initiation of or Increase in Cardiac Medications
Adverse Events

Full Information

First Posted
June 21, 2005
Last Updated
February 1, 2018
Sponsor
Carelon Research
Collaborators
National Heart, Lung, and Blood Institute (NHLBI)
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1. Study Identification

Unique Protocol Identification Number
NCT00115349
Brief Title
Combination Therapy Compared With Single-Drug Therapy in Patients With Cardiac Diseases
Official Title
Thalassemia Clinical Research Network - Cardiac L1/DFO Trial
Study Type
Interventional

2. Study Status

Record Verification Date
January 2014
Overall Recruitment Status
Terminated
Why Stopped
due to low enrollment
Study Start Date
June 2005 (undefined)
Primary Completion Date
July 2008 (Actual)
Study Completion Date
April 2009 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Carelon Research
Collaborators
National Heart, Lung, and Blood Institute (NHLBI)

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The purpose of this study is to determine whether left ventricular function improves more rapidly with deferoxamine (DFO) and deferiprone (L1) combination therapy than with DFO monotherapy in patients with thalassemia and decreased ejection fractions. Secondary aims include evaluating changes in myocardial iron burden using T2* and estimating the relative incidence and severity of chelator-induced toxicity.
Detailed Description
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.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Cardiovascular Diseases, Heart Diseases, Beta-Thalassemia

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigator
Allocation
Randomized
Enrollment
20 (Actual)

8. Arms, Groups, and Interventions

Arm Title
L1/DFO
Arm Type
Experimental
Arm Description
Deferoxamine (DFO) and deferiprone (L1) combination therapy
Arm Title
DFO
Arm Type
Active Comparator
Arm Description
Deferoxamine (DFO) monotherapy
Intervention Type
Drug
Intervention Name(s)
Deferoxamine
Other Intervention Name(s)
DFO
Intervention Description
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.
Intervention Type
Drug
Intervention Name(s)
Deferiprone (L1)
Other Intervention Name(s)
L1
Intervention Description
The dose of L1, 75mg/kg in three divided oral doses, is the maximum dose at which toxicity has been tested in prospective trials
Primary Outcome Measure Information:
Title
Change in Left Ventricular Ejection Fraction (LVEF).
Description
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.
Time Frame
Baseline to one year
Secondary Outcome Measure Information:
Title
Evaluate Whether L1/DFO Combination Therapy is Superior to DFO Monotherapy in Lowering Myocardial Iron Burden Estimated by Myocardial T2*.
Time Frame
one year
Title
Change in Left Ventricular (LV) Volume From Screening to One Year.
Time Frame
one year
Title
Change in ECHO LV Volume, Ejection Fraction, Shortening Fraction, and VCFc/Wall Stress Z-score From Baseline to One Year.
Time Frame
one year
Title
Change in Holter Monitor Scores From Baseline to One Year.
Time Frame
one year
Title
Initiation of or Increase in Cardiac Medications
Time Frame
continuous
Title
Adverse Events
Time Frame
continous

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
100 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
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)
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
John Porter, MD
Organizational Affiliation
University College, London
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Patricia J. Giardina, MD
Organizational Affiliation
Weill Medical College of Cornell University
Official's Role
Study Chair
First Name & Middle Initial & Last Name & Degree
Ellis J. Neufeld, MD
Organizational Affiliation
Boston Children's Hospital
Official's Role
Study Chair
First Name & Middle Initial & Last Name & Degree
Elliott P, Vichinsky, MD
Organizational Affiliation
Children's Hospital and Research Institute, Oakland
Official's Role
Study Chair
First Name & Middle Initial & Last Name & Degree
Sonja McKinlay, Ph.D.
Organizational Affiliation
New England Research Institutes, Inc.
Official's Role
Study Chair
Facility Information:
Facility Name
Children's Hospital of Los Angeles
City
Los Angeles
State/Province
California
ZIP/Postal Code
90027
Country
United States
Facility Name
Children's Hospital
City
Oakland
State/Province
California
ZIP/Postal Code
94609
Country
United States
Facility Name
Children's Memorial Hospital
City
Chicago
State/Province
Illinois
ZIP/Postal Code
60614-3394
Country
United States
Facility Name
Children's Hospital
City
Boston
State/Province
Massachusetts
ZIP/Postal Code
02115
Country
United States
Facility Name
Weill Medical College of Cornell University
City
New York
State/Province
New York
ZIP/Postal Code
10021
Country
United States
Facility Name
Children's Hospital of Philadelphia
City
Philadelphia
State/Province
Pennsylvania
ZIP/Postal Code
19104-4399
Country
United States

12. IPD Sharing Statement

Learn more about this trial

Combination Therapy Compared With Single-Drug Therapy in Patients With Cardiac Diseases

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