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A B C D E F G H I J K L M N O P Q R S T U V W X Y ZClinical Trials for Hemoglobinopathies
- Pre-transplant Immunosuppression and Donor Stem Cell Transplant for the Treatment of Severe Hemoglobinopathies
- Cord Blood Transplant in Children and Young Adults With Blood Cancers and Non-malignant Disorders
- Long Term Follow-up Study for Patients Enrolled on the BP-004 Clinical Study
- Study of Gene Modified Donor T-cells Following TCR Alpha Beta Positive Depleted Stem Cell Transplant
- A Blood Stem Cell Transplant for Sickle Cell Disease
- Reduced Intensity Conditioning and Familial HLA-Mismatched BMT for Non-Malignant Disorders
- Fetal Hemoglobin Induction Treatment Metformin
- HSCT For Patients With High Risk Hemoglobinopathies Using Reduced Intensity
- Treosulfan-based Versus Busulfan-based Conditioning in Paediatric Patients With Non-malignant Diseases
- Hematopoietic Stem Cell Transplant for High Risk Hemoglobinopathies
- Combined Bone Marrow and Renal Transplantation for Hematologic Disorders With End Stage Renal Disease
- Safety Study of Gene Modified Donor T-cells Following TCR Alpha Beta Depleted Stem Cell Transplant
- Non-Myeloablative Conditioning and Bone Marrow Transplantation
- Efficacy/Safety Study of Deferiprone Compared to Deferasirox in Paediatric Patients
- Pharmacokinetic Study of Deferiprone in Paediatric Patients
- Second or Greater Allogeneic Hematopoietic Stem Cell Transplant Using Reduced Intensity Conditioning (RIC)
- Allogeneic SCT of NiCord®, UCB-Derived Ex Vivo Expanded Stem and Progenitor Cells, in Patients With Hemoglobinopathies
- Reduced Intensity Conditioning (RIC) Regimen for Patients With Non-malignant Disorders
- Campath/Fludarabine/Melphalan Transplant Conditioning for Non-Malignant Diseases
- Interferon and Ribavirin Treatment in Patients With Hemoglobinopathies
- Reduced Intensity Conditioning for Umbilical Cord Blood Transplant in Pediatric Patients With Non-Malignant Disorders
- Magnetic Resonance Imaging (MRI) Assessments of the Heart and Liver Iron Load in Patients With Transfusion Induced Iron Overload
- Bone Marrow Transplantation, Hemoglobinopathies, SCALLOP
- Stem Cell Transplant for Hemoglobinopathy
- Allogeneic Stem Cell Transplantation Following Chemotherapy in Patients With Hemoglobinopathies
- Bone Marrow Transplant From Related Donor for Patients With High Risk Hemoglobinopathies
- Bone Marrow Transplant From Donor Using Less Toxic Conditioning for Patient With High Risk Hemoglobinopathies
- Stem Cell Transplantation After Reduced-Dose Chemotherapy for Patients With Sickle Cell Disease or Thalassemia
- Allogeneic Mixed Chimerism Stem Cell Transplant Using Campath for Hemoglobinopathies & Bone Marrow Failure Syndromes
- Hydroxyurea to Treat Beta-Thalassemia (Cooley's Anemia)
- Pediatric Hydroxyurea in Sickle Cell Anemia (PED HUG)
- Evaluation of Subcutaneous Desferrioxamine as Treatment for Transfusional Hemochromatosis
- Chelation Therapy of Iron Overload With Pyridoxal Isonicotinoyl Hydrazone
- Multicenter Study of Hydroxyurea in Patients With Sickle Cell Anemia (MSH)
- Penicillin Prophylaxis in Sickle Cell Disease (PROPS)