- Trials with a EudraCT protocol (4,317)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (4)
4,317 result(s) found for: Blood Cell.
Displaying page 1 of 216.
EudraCT Number: 2020-004225-22 | Sponsor Protocol Number: CSEG101A2401B | Start Date*: 2021-05-03 | ||||||||||||||||
Sponsor Name:Novartis Pharma AG | ||||||||||||||||||
Full Title: An Open-label, Multi-center, Phase IV, Rollover Study for Patients with Sickle Cell Disease who have Completed a Prior Novartis-Sponsored Crizanlizumab Study | ||||||||||||||||||
Medical condition: Sickle Cell Disease | ||||||||||||||||||
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Population Age: Infants and toddlers, Children, Adolescents, Under 18, Adults | Gender: Male, Female | |||||||||||||||||
Trial protocol: BE (Trial now transitioned) DE (Trial now transitioned) ES (Ongoing) IT (Ongoing) FR (Trial now transitioned) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-004568-37 | Sponsor Protocol Number: INV543 | Start Date*: 2018-11-30 | ||||||||||||||||
Sponsor Name:Nova Laboratories Limited | ||||||||||||||||||
Full Title: A prospective open label, pharmacokinetic study of an oral hydroxyurea solution in children with sickle cell anemia | ||||||||||||||||||
Medical condition: Sickle Cell Anaemia | ||||||||||||||||||
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Population Age: Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | |||||||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-004045-25 | Sponsor Protocol Number: GBT440-034 | Start Date*: 2018-04-17 | |||||||||||
Sponsor Name:Global Blood Therapeutics, Inc. | |||||||||||||
Full Title: An Open Label Extension Study of Voxelotor (GBT440) Administered Orally to Participants with Sickle Cell Disease Who Have Participated in Voxelotor Clinical Trials | |||||||||||||
Medical condition: Sickle Cell Disease | |||||||||||||
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Population Age: Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) FR (Completed) NL (Ongoing) IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-005889-40 | Sponsor Protocol Number: ABR-15108 | Start Date*: 2007-08-14 | |||||||||||
Sponsor Name:Academic Medical Centre | |||||||||||||
Full Title: N-Acetylcysteine for Treatment of Sickle Cell Disease | |||||||||||||
Medical condition: Patients homozygous for sickle cell disease | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2020-003601-66 | Sponsor Protocol Number: CSEG101ANL01T | Start Date*: 2021-07-14 | |||||||||||
Sponsor Name:Amsterdam UMC - AMC | |||||||||||||
Full Title: The Effect of Crizanlizumab on Cerebral Perfusion and Oxygenation in Sickle Cell Patients | |||||||||||||
Medical condition: Sickle Cell Disease | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2022-001585-36 | Sponsor Protocol Number: AMC_SMILE_1.0 | Start Date*: Information not available in EudraCT | |||||||||||
Sponsor Name:Amsterdam UMC | |||||||||||||
Full Title: EffectS of L-glutaMIne on oxIdative stress, sickLE erythrocyte viability, inflammation and endothelial activity in sickle cell disease (SMILE trial) | |||||||||||||
Medical condition: Sickle Cell Disease | |||||||||||||
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Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2021-001351-13 | Sponsor Protocol Number: APHP201133 | Start Date*: 2021-11-26 | |||||||||||
Sponsor Name:Assistance Publique des Hôpitaux de Paris(AP-HP) | |||||||||||||
Full Title: Interest of famotidine in reducing endothelial expression of P-selectin in children with sickle cell disease: pilot study, single-center, prospective, non-comparative | |||||||||||||
Medical condition: major sickle cell syndrome | |||||||||||||
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Population Age: Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-005161-20 | Sponsor Protocol Number: SCC01 | Start Date*: 2012-02-14 | |||||||||||
Sponsor Name:University College Dublin Clinical Research Centre | |||||||||||||
Full Title: A Randomised Controlled Double-Blind Trial of Intranasal Fentanyl versus Intravenous Morphine in the Emergency Department Treatment of Severe Painful Sickle Cell Crises in Children | |||||||||||||
Medical condition: Severe Painful Sickle Cell Disease Crises in Children | |||||||||||||
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Population Age: Infants and toddlers, Children, Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
Trial protocol: IE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2020-005289-32 | Sponsor Protocol Number: GBT2104-133 | Start Date*: 2021-11-10 | |||||||||||
Sponsor Name:Global Blood Therapeutics, Inc. | |||||||||||||
Full Title: An Open-Label Extension Study to Evaluate the Long-Term Safety of Inclacumab Administered to Participants with Sickle Cell Disease Who Have Participated in an Inclacumab Clinical Trial | |||||||||||||
Medical condition: Sickle Cell Disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2019-001838-34 | Sponsor Protocol Number: GBT440-029 | Start Date*: 2019-11-05 | |||||||||||
Sponsor Name:Global Blood Therapeutics, Inc. | |||||||||||||
Full Title: A Phase 2, Open Label, Multiple Dose Escalation Study to Evaluate the Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of Voxelotor in Patients with Sickle Cell Disease | |||||||||||||
Medical condition: Sickle Cell Disease | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-003573-41 | Sponsor Protocol Number: 1101-202 | Start Date*: 2009-01-15 | |||||||||||
Sponsor Name:TRF Pharma, Inc. | |||||||||||||
Full Title: A randomised, double-blind, placebo-controlled study to assess the safety and activity of TRF-1101 on microvascular blood flow, vascular endothelial injury, and vasoocclusive pain in patients with ... | |||||||||||||
Medical condition: Sickle cell disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Prematurely Ended) FR (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2016-004209-15 | Sponsor Protocol Number: GBT440-007 | Start Date*: 2019-01-08 | |||||||||||
Sponsor Name:Global Blood Therapeutics, Inc. | |||||||||||||
Full Title: A Phase 2a, Open-label, Single and Multiple Dose Study to Evaluate the Pharmacokinetics, Safety, Tolerability and Treatment Effect of GBT440 in Pediatric Participants with Sickle Cell Disease | |||||||||||||
Medical condition: Sickle Cell Disease | |||||||||||||
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Population Age: Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2020-003485-39 | Sponsor Protocol Number: NN7533-4470 | Start Date*: 2022-07-19 | |||||||||||
Sponsor Name:Novo Nordisk A/S | |||||||||||||
Full Title: A multicentre trial evaluating the efficacy and safety of oral decitabine-tetrahydrouridine (NDec) in patients with sickle cell disease | |||||||||||||
Medical condition: Sickle cell disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GR (Ongoing) IT (Ongoing) ES (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2010-022812-37 | Sponsor Protocol Number: ORH/PID/6265 | Start Date*: 2011-06-07 | |||||||||||
Sponsor Name:Oxford University Hospitals NHS Trust | |||||||||||||
Full Title: A phase 2 trial of AZD1152 in relapsed/refractory diffuse large B-cell lymphoma | |||||||||||||
Medical condition: Diffuse Large B-cell Lymphoma (DLBCL) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2019-003144-76 | Sponsor Protocol Number: GBT440-038 | Start Date*: 2020-01-10 | |||||||||||
Sponsor Name:Global Blood Therapeutics, Inc. | |||||||||||||
Full Title: An Open-Label Extension Study of Voxelotor Administered Orally to Pediatric Participants with Sickle Cell Disease Who Have Participated in Voxelotor Clinical Trials | |||||||||||||
Medical condition: Sickle Cell Disease | |||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2010-023040-32 | Sponsor Protocol Number: ROMI-ADVM-004 | Start Date*: 2011-05-05 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Sponsor Name:Celgene Corporation | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Full Title: A phase IV, Open-Label, Single-Arm ROLLOVER STUDY FOR SUBJECTS WHO PARTICIPATED IN OTHER ROMIDEPSIN PROTOCOLS. Estudio de extensión de fase IV, abierto, de un solo brazo para pacientes que hayan p... | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Medical condition: Rollover study supporting all indications from prior Romidepsin protocols eligible for participation in this study. Estudio de extensión que recoge todas las indicaciones de protocolos anteriores d... | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Trial protocol: ES (Prematurely Ended) GB (Completed) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2011-005371-16 | Sponsor Protocol Number: D4302C00001 | Start Date*: 2012-07-30 | |||||||||||
Sponsor Name:Rigel Pharmaceuticals, Inc. | |||||||||||||
Full Title: Phase II Trial to Evaluate the Efficacy of Fostamatinib in Patients with Relapsed or Refractory Diffuse Large B-Cell Lymphoma (DLBCL) | |||||||||||||
Medical condition: Diffuse Large B-cell Lymphoma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2018-002605-62 | Sponsor Protocol Number: BCC1801 | Start Date*: 2018-10-23 | |||||||||||
Sponsor Name:Herlev and Gentofte Hospital | |||||||||||||
Full Title: Phase IIa trial with PD-L1 IO103 vaccination with montanide in patients with basal cell carcinoma. | |||||||||||||
Medical condition: basal cell carcinoma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2021-000932-70 | Sponsor Protocol Number: APHP200067 | Start Date*: Information not available in EudraCT | |||||||||||
Sponsor Name:ASSISTANCE PUBLIQUE -HOPITAUX DE PARIS | |||||||||||||
Full Title: Randomized prospective trial evaluating the efficacy of the antiCD38 monoclonal antibody isatuximab in the treatment of PCRA by major ABO mismatch after allogeneic hematopoietic stem cell transplan... | |||||||||||||
Medical condition: Pure cell red aplasia by major ABO mismatch after allogeneic hematopoietic stem cell transplantation | |||||||||||||
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Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2010-021165-76 | Sponsor Protocol Number: LU2006 | Start Date*: 2011-09-19 | |||||||||||
Sponsor Name:Sheffield Teaching Hospitals NHS Foundation Trust | |||||||||||||
Full Title: STOMP: Small cell lung cancer Trial of Olaparib (AZD2281) as Maintenance Programme: a randomised, double blind, multicentre phase II trial | |||||||||||||
Medical condition: Small cell lung cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) | |||||||||||||
Trial results: View results |
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