HSCT For Patients With High Risk Hemoglobinopathies Using Reduced Intensity
Completed · Phase 1/Phase 2
Conditions studied: Sickle Cell Disease, Beta Thalassemia-Major
In brief
This study will evaluate the use of reduced intensity conditioning regimen in patients with high risk hemoglobinopathy Sickle Cell and B-Thalassemia Major in combination with standard immunosuppressive medications, followed by a routine stem cell transplant in order to assess whether or not it is as effective as myeloablative high dose chemotherapy and transplant.
Key facts
- Study ID
- NCT02435901
- Run by
- Northwell Health
- People needed
- 29
- Starts
- 2008-12-01
- Expected to finish
- 2019-12-01
- Last updated by the study team
- 2021-08-24
Who can join
Age: 1 and older, up to 21. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Patient Inclusion Criteria for Sickle Cell Disease
- Patients at least one year of age to less than or equal to 21 years of age with (Sickle Cell Disease-SS or Sickle Cell-S-β-Thalassemia and with one or more of the following disease complications:
- Development of stroke on chronic transfusion protocol.
- Allosensitization on chronic transfusion therapy
- Impaired neuropsychological function and abnormal MRI scan
- Abnormal Transcranial Doppler studies
- Acute chest syndrome (2 to 3 episodes of acute chest syndrome in last 3 to 4 years).
- Ferritin level < 1500 mg/ml
- Recurrent painful priapism; 3-4 episodes/year requiring intervention.
- Recurrent vaso-occlusive crisis of at least 3 to 4 episodes/year.
- Osteonecrosis of multiple bones with documented destructive changes.
- Signed informed consent
- Patients physically and psychologically capable of undergoing transplantation and a period of strict isolation.
- Ferritin < 1500
- Liver Iron Concentration < 6mg/g
- Patient Inclusion Criteria for β Thalassemia major Patients less than or equal to 21 years of age with B- Thalassemia major on routine monthly transfusion protocol or with one or more of the following complications;
- Hepatomegaly.
- Liver biopsy revealing evidence of portal fibrosis as A) Mild B) Moderate
- Ferritin level≤ 1500ng/ml
- Liver Iron Concentration (LIC) < 6mg/g
You may not qualify if…
- Exclusion Criteria for Both Sickle Cell and β Thalassemia Major Patient
- HIV positive result confirmed by Western Blot.
- Pregnancy (Pregnancy testing for females of child-bearing age will be performed and those with a positive serum β-Human Chorionic Gonadotropin will be excluded) and lactating females.
- Creatinine greater than two times the upper limit of normal for the laboratory,
- Pulmonary disease with FVC, FEV1 or DLCO parameters < 50% predicted (corrected for hemoglobin) or stage 3 or 4 sickle lung disease.
- Cardiac insufficiency or coronary artery disease requiring treatment
- Active infection requiring systemic antibiotic therapy with antibacterial, antifungal or antiviral agents
- Lansky performance score <70%- (Appendix B)
- Acute hepatitis/biopsy evidence of cirrhosis.
- Pulmonary Hypertension
Where it is running
- Cohen Children's Medical Center of New York — New Hyde Park, New York, United States
Full record on ClinicalTrials.gov
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