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Hydroxyurea to Treat Beta-Thalassemia (Cooley's Anemia)

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ClinicalTrials.gov Identifier: NCT00001958
Recruitment Status : Completed
First Posted : January 19, 2000
Last Update Posted : March 4, 2008
Sponsor:
Information provided by:
National Institutes of Health Clinical Center (CC)

Study Description
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Brief Summary:

This 12-month study will evaluate the safety and effectiveness of hydroxyurea in treating beta-thalassemia, a type of anemia caused by defective hemoglobin (the oxygen-carrying pigment in blood). Hemoglobin is composed of two protein chains-alpha globin chains and beta globin chains; patients with beta-thalassemia do not make beta globin. Patients often require frequent red blood cell transfusions. This leads to iron overload, which, in turn, requires iron chelation therapy (removal of iron from the blood).

Some drugs, including hydroxyurea, can stimulate production of a third type of protein chain called gamma chains. In the womb, the fetus makes this type of protein instead of beta globin. It is not until after birth, when the fetus no longer produces gamma globin that the beta globin deficiency becomes apparent. Gamma chain synthesis improves hemoglobin and red blood cell production, correcting the anemia. This study will determine if and at what dose hydroxyurea treatment reduces patients' need for red blood cell transfusions and whether certain factors might predict which patients are likely benefit from this treatment.

Patients 15 years and older with moderately severe beta-thalassemia may be eligible for this study. Participants will take hydroxyurea daily at a dose calculated according to the patient's body size. Blood will be drawn weekly to measure blood cell and platelet counts. The drug dosage may be increased after 12 weeks of treatment and again after 24 weeks if the white cell and platelet counts remain stable. Patients who respond dramatically to treatment may continue to receive hydroxyurea for up to 3 years.


Condition or disease Intervention/treatment Phase
Beta Thalassemia Hemoglobinopathy Drug: Hydroxyurea Phase 2

Detailed Description:
Individuals with homozygous beta thalassemia are either severely anemic or dependent on blood transfusion to sustain life. Deficient synthesis of the beta chain leads to imbalanced chain synthesis with an excess of alpha globin. This alpha globin precipitates, causing ineffective erythropoiesis and shortened red cell survival. Hydroxyurea is a cell-cycle specific agent that blocks DNA synthesis by inhibiting ribonuclease reductase, the enzyme that converts ribonucleotides to deoxyribonucleotides. Administration of hydroxyurea to primates and more than 300 patients with sickle cell anemia has been frequently, but not invariably associated with a substantial increase in synthesis of gamma globin. In patients with homozygous beta-thalassemia, enhanced gamma globin synthesis could partially compensate for the deficient synthesis of beta globin rendering chain synthesis more balanced and reducing the relative excess of alpha chains. The purpose of this protocol is to test the hypothesis that chronic daily low dose administration of hydroxyurea will enhance gamma globin synthesis, increase red cell production and partially or substantially correct the anemia in patients with homozygous beta-thalassemia. The effect of treatment will be monitored by serial determination of the hemoglobin and hematocrit. The relationship between response to therapy and the specific beta-globin mutation(s) will also be analyzed. This study will therefore examine a cohort of patients not previously treated with hydroxyurea.
Study Design
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Study Type : Interventional  (Clinical Trial)
Enrollment : 100 participants
Primary Purpose: Treatment
Official Title: Effect of Hydroxyurea on the Level of Ineffective Erythropoiesis, Transfusion Requirement, and Fetal Hemoglobin Synthesis in Patients With Beta-Thalassemia-Intermedia
Study Start Date : December 1999
Study Completion Date : February 2002

Resource links provided by the National Library of Medicine

MedlinePlus related topics: Anemia Thalassemia
Drug Information available for: Hydroxyurea

Arms and Interventions
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Outcome Measures
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Eligibility Criteria
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Information from the National Library of Medicine

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Ages Eligible for Study:   Child, Adult, Older Adult
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Criteria

Beta-Thalassemia Intermedia patients.

Steady-state Hb values greater than 6.5gm/dl (unrelated to transfusion)

Males and females.

Patients greater than 15 years of age.

Patients who are transfusion-requiring but not dependent will be offered the opportunity to enroll.

Stable renal and hepatic function

Willingness to use appropriate birth control measures.

Ability to give informed consent.

No beta-thalassemia major.

No blood transfusion requirement greater than 1 unit every 2 months over the last 12 months.

No patients with WBC less than 4000/micrograms.

No one with a platelet count less than 150,000/micrograms.

No evidence of active viral infective, including viral hepatitis.

No abnormal liver function test (ALT or AST greater than 2.5 x normal).

No abnormal renal function test (creatinine greater 1.5 mg/dl).

No HIV positive blood test.

Contacts and Locations
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Information from the National Library of Medicine

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): NCT00001958


Locations
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United States, Maryland
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Bethesda, Maryland, United States, 20892
Sponsors and Collaborators
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
More Information
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Publications:

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ClinicalTrials.gov Identifier: NCT00001958    
Other Study ID Numbers: 000040
00-DK-0040
First Posted: January 19, 2000    Key Record Dates
Last Update Posted: March 4, 2008
Last Verified: February 2002
Keywords provided by National Institutes of Health Clinical Center (CC):
Gamma Gene
Hemoglobin Switching
Erythropoiesis
 HbE Hemoglobin Chain Synthesis Imbalance
Cooley's Anemia
Beta-Thalassemia Intermedia
Additional relevant MeSH terms:
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Thalassemia
beta-Thalassemia
Hemoglobinopathies
Anemia, Hemolytic, Congenital
Anemia, Hemolytic
Anemia
Hematologic Diseases
 Genetic Diseases, Inborn
Hydroxyurea
Antineoplastic Agents
Antisickling Agents
Enzyme Inhibitors
Molecular Mechanisms of Pharmacological Action
Nucleic Acid Synthesis Inhibitors