- Trials with a EudraCT protocol (1,656)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
1,656 result(s) found for: Beta 1.
Displaying page 1 of 83.
EudraCT Number: 2009-014136-37 | Sponsor Protocol Number: Thal-002 | Start Date*: 2010-07-13 | |||||||||||||||||||||
Sponsor Name:University of Washington | |||||||||||||||||||||||
Full Title: A pilot study on the safety and efficacy of haemopoietic stem cell mobilization (CD34+ cells) with MOZOBIL ± G-CSF, in adult patients diagnosed with beta-thalassaemia major. | |||||||||||||||||||||||
Medical condition: Beta-thalassaemia major | |||||||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: GR (Completed) | |||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2018-001469-18 | Sponsor Protocol Number: CT2-04-17 | Start Date*: 2019-04-17 | ||||||||||||||||
Sponsor Name:Dipartimento di Scienze della Vita e Biotecnologie dell'Università degli Studi di Ferrara | ||||||||||||||||||
Full Title: Treatment of beta-thalassemia patients with rapamycin (sirolimus): from pre-clinical research to a clinical trial | ||||||||||||||||||
Medical condition: Beta-thalassemia transfusion dependent patients | ||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | |||||||||||||||||
Trial protocol: IT (Completed) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2022-002395-36 | Sponsor Protocol Number: P-SP420-THAL-01 | Start Date*: 2022-12-16 | |||||||||||
Sponsor Name:Pharmacosmos A/S | |||||||||||||
Full Title: An open-label, dose-escalation, dose-finding, and proof-of-concept trial of SP-420 in subjects with transfusion-dependent β-thalassemia | |||||||||||||
Medical condition: Transfusion-dependent β-thalassemia | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Trial now transitioned) GR (Trial now transitioned) IT (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2018-001942-33 | Sponsor Protocol Number: CT2-02-17 | Start Date*: 2019-01-23 | |||||||||||
Sponsor Name:Rare Partners s.r.l. Impresa Sociale | |||||||||||||
Full Title: A personalized medicine approach for beta-thalassemia transfusion dependent patients: testing SIROLIMUS in a first pilot clinical trial. | |||||||||||||
Medical condition: beta-thalassemic patients | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-000973-30 | Sponsor Protocol Number: AMD-THAL | Start Date*: 2011-04-28 | |||||||||||
Sponsor Name:FONDAZIONE CENTRO S. RAFFAELE DEL MONTE TABOR | |||||||||||||
Full Title: PLERIXAFOR MOBILIZED STEM CELLS AS SOURCE FOR GENE THERAPY OF BETA-THALASSEMIA AMD-THAL . | |||||||||||||
Medical condition: transfusion dependent beta thalassemia | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2019-000208-13 | Sponsor Protocol Number: ACE-536-B-THAL-004 | Start Date*: 2019-12-09 | |||||||||||
Sponsor Name:Celgene Corporation | |||||||||||||
Full Title: A phase 2a study to evaluate the safety and pharmacokinetics of Luspatercept (ACE-536) in paediatric participants who require regular red blood cell transfusions due to beta (β) thalassemia | |||||||||||||
Medical condition: Beta-Thalassemia | |||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Trial now transitioned) GR (Trial now transitioned) IT (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2016-003611-35 | Sponsor Protocol Number: HGB-212 | Start Date*: 2017-07-24 | |||||||||||
Sponsor Name:bluebird bio, Inc. | |||||||||||||
Full Title: A Phase 3 Single Arm Study Evaluating the Efficacy and Safety of Gene Therapy in Subjects with Transfusion-dependent β-Thalassemia, by Transplantation of Autologous CD34+ Stem Cells Transduced Ex V... | |||||||||||||
Medical condition: This study will enroll subjects with transfusion dependent beta-thalassemia, defined by a history of at least 100 mL/kg/year of packed red blood cells (pRBCs) or ≥ 8 transfusions of pRBCs per year... | |||||||||||||
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Population Age: Children, Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) DE (Completed) GR (Completed) FR (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-001936-12 | Sponsor Protocol Number: MD2014.01 | Start Date*: 2019-02-11 | ||||||||||||||||
Sponsor Name:Sanquin Plasma Products BV | ||||||||||||||||||
Full Title: Efficacy and Safety of human apotransferrin in patients with β-thalassemia | ||||||||||||||||||
Medical condition: Beta thalassemia intermedia | ||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | |||||||||||||||||
Trial protocol: NL (Prematurely Ended) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2015-004122-33 | Sponsor Protocol Number: HGB-207 | Start Date*: 2016-11-10 | |||||||||||
Sponsor Name:bluebird bio, Inc. | |||||||||||||
Full Title: A Phase 3 Single Arm Study Evaluating the Efficacy and Safety of Gene Therapy in Subjects with Transfusion-dependent β-Thalassemia, who do not have β0/β0 Genotype, by Transplantation of Autologous ... | |||||||||||||
Medical condition: This study will enroll subjects with transfusion dependent beta-thalassemia, who do not have beta0/beta0 genotype, defined by a history of at least 100 mL/kg/year of packed red blood cells (pRBCs) ... | |||||||||||||
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Population Age: Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) DE (Completed) GR (Completed) GB (GB - no longer in EU/EEA) FR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-002499-15 | Sponsor Protocol Number: A536-04 | Start Date*: 2012-12-19 | ||||||||||||||||
Sponsor Name:ACCELERON PHARMA INC | ||||||||||||||||||
Full Title: A Phase 2, Open-Label, Ascending Dose Study to Evaluate the Effects of ACE-536 in Patients with β-Thalassemia Intermedia | ||||||||||||||||||
Medical condition: β-thalassemia intermedia | ||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | |||||||||||||||||
Trial protocol: IT (Completed) GR (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2021-002172-39 | Sponsor Protocol Number: VX21-CTX001-141 | Start Date*: 2021-10-05 | |||||||||||
Sponsor Name:VERTEX PHARMACEUTICALS INCORPORATED | |||||||||||||
Full Title: A Phase 3 Study to Evaluate the Safety and Efficacy of a Single Dose of CTX001 in Pediatric Subjects With Transfusion-Dependent ß-Thalassemia | |||||||||||||
Medical condition: Transfusion-Dependent ß Thalassemia | |||||||||||||
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Population Age: Children, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Trial now transitioned) DE (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2014-004860-39 | Sponsor Protocol Number: TIGET-BTHAL | Start Date*: 2015-03-04 | |||||||||||
Sponsor Name:OSPEDALE SAN RAFFAELE | |||||||||||||
Full Title: A phase I/II study evaluating safety and efficacy of autologous hematopoietic stem cells genetically modified with GLOBE lentiviral vector encoding for the human beta-globin gene for the treatment ... | |||||||||||||
Medical condition: Beta talassemia trasfusione dipendente | |||||||||||||
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Population Age: Children, Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2015-003535-35 | Sponsor Protocol Number: CICL670A0106E1 | Start Date*: 2016-03-08 | ||||||||||||||||
Sponsor Name:Novartis Pharma AG | ||||||||||||||||||
Full Title: A 4-year Extension to a Phase II a Multicenter Study Evaluating Long-term Safety, Tolerability, Pharmacokinetics and Effects on Liver Iron Concentration of Repeated Doses of 10 mg/kg/Day of Deferas... | ||||||||||||||||||
Medical condition: | ||||||||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | |||||||||||||||||
Trial protocol: Outside EU/EEA | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2014-001281-94 | Sponsor Protocol Number: A536-06 | Start Date*: 2015-03-11 | |||||||||||||||||||||
Sponsor Name:Acceleron Pharma, Inc. | |||||||||||||||||||||||
Full Title: An Open-Label Extension Study to Evaluate the Long-Term Effects of ACE-536 in Patients with β-Thalassemia Previously Enrolled in Study A536-04 | |||||||||||||||||||||||
Medical condition: β-Thalassemia Intermedia and β-Thalassemia major | |||||||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: IT (Completed) GR (Completed) | |||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2009-013284-19 | Sponsor Protocol Number: HINABS-ITI | Start Date*: 2009-12-10 |
Sponsor Name:Medical University Innsbruck | ||
Full Title: Immune tolerance induction in MS patients with neutralizing antibodies against interferon-beta | ||
Medical condition: multiple sclerosis patients with neutralizing antibodies against interferon-beta | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: AT (Completed) | ||
Trial results: View results |
EudraCT Number: 2010-020357-14 | Sponsor Protocol Number: CCFM154/310 | Start Date*: 2011-05-16 |
Sponsor Name:FONDAZIONE MONZINO CENTRO CARDIOLOGICO | ||
Full Title: EFFECTS OF BETA 2 RECEPTOR BLOCKADE ON PULMONARY FUNCTION IN A HUMAN MODEL OF ACUTE HYDRIC OVERLOAD | ||
Medical condition: BETA BLOCKADE AND LUNG FUNCTION | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: IT (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2017-003351-38 | Sponsor Protocol Number: CTX001-111 | Start Date*: 2018-07-25 | |||||||||||
Sponsor Name:Vertex Pharmaceuticals Incorporated | |||||||||||||
Full Title: A Phase 1/2/3 Study of the Safety and Efficacy of a Single Dose of Autologous CRISPR-Cas9 Modified CD34+ Human Hematopoietic Stem and Progenitor Cells (hHSPCs) in Subjects with Transfusion-Dependen... | |||||||||||||
Medical condition: Transfusion-Dependent β Thalassemia | |||||||||||||
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Population Age: Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Trial now transitioned) IT (Completed) GB (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2005-001008-37 | Sponsor Protocol Number: Bab1 | Start Date*: 2005-11-01 |
Sponsor Name:Sahlgrenska University Hospital | ||
Full Title: Analysis of the antibody level against interferon beta before and after increase of dose in MS therapy | ||
Medical condition: Multiple sclerosis | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: SE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2004-005261-38 | Sponsor Protocol Number: AVS00103 | Start Date*: 2005-10-04 | |||||||||||
Sponsor Name:Genzyme Europe BV | |||||||||||||
Full Title: A Multicenter, Parallel, Double-Blind, Blinded Evaluator, Randomized Comparison of the Efficacy and Safety of an Alternate Viscosupplement (AVS-beta) to Methylprednisolone Acetate in Patients with ... | |||||||||||||
Medical condition: Osteoarthritis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2021-006390-37 | Sponsor Protocol Number: VX21-CTX001-161 | Start Date*: Information not available in EudraCT | ||||||||||||||||
Sponsor Name:Vertex Pharmaceuticals Incorporated | ||||||||||||||||||
Full Title: A Phase 3b Study to Evaluate Efficacy and Safety of a Single Dose of Autologous CRISPR Cas9 Modified CD34+ Human Hematopoietic Stem and Progenitor Cells (CTX001) in Subjects with Transfusion-Depend... | ||||||||||||||||||
Medical condition: Transfusion-dependent β-thalassemia (TDT) and severe sickle cell disease (SCD) | ||||||||||||||||||
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Population Age: Adolescents, Under 18, Adults | Gender: Male, Female | |||||||||||||||||
Trial protocol: DE (Trial now transitioned) IT (Trial now transitioned) | ||||||||||||||||||
Trial results: (No results available) |
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