- Trials with a EudraCT protocol (3,331)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
3,331 result(s) found for: Cell count.
Displaying page 1 of 167.
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: 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: 2006-005566-39 | Sponsor Protocol Number: 06_DOG07_64 | Start Date*: 2008-03-05 | ||||||||||||||||
Sponsor Name:Christie Hospital NHS Foundation Trust | ||||||||||||||||||
Full Title: Concurrent chemoradiotherapy for stage III non small cell lung cancer followed by consolidation pemetrexed: a phase II study | ||||||||||||||||||
Medical condition: Non-small cell lung cancer, stage III | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: GB (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2006-002987-24 | Sponsor Protocol Number: 152CL201 | Start Date*: 2007-06-25 | |||||||||||
Sponsor Name:Biogen Idec Ltd | |||||||||||||
Full Title: A Randomized, Open-Label, Multicenter, Phase 2 Study to Evaluate the Safety and Efficacy of Lumiliximab in Combination with Fludarabine, Cyclophosphamide, and Rituximab Versus Fludarabine, Cyclopho... | |||||||||||||
Medical condition: Relapsed Chronic Lymphocytic Leukemia (CLL) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) AT (Prematurely Ended) ES (Completed) IT (Prematurely Ended) FR (Completed) DE (Prematurely Ended) GB (Completed) CZ (Prematurely Ended) SK (Completed) PT (Prematurely Ended) LT (Prematurely Ended) GR (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-007139-26 | Sponsor Protocol Number: S075LBH501 | Start Date*: 2008-04-17 | |||||||||||
Sponsor Name:SENDO TECH | |||||||||||||
Full Title: A phase II study of the histone deacetylase inhibitor Panobinostat (LBH589) in patients with advanced Small Cell Lung Cancer (SCLC) | |||||||||||||
Medical condition: SCLC patients | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) DE (Completed) GR (Prematurely Ended) | |||||||||||||
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 (Trial now transitioned) IT (Trial now transitioned) ES (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2005-003796-20 | Sponsor Protocol Number: HOVON 77 | Start Date*: 2007-01-03 | |||||||||||
Sponsor Name:HOVON Foundation | |||||||||||||
Full Title: Efficacy and safety of a single dose of 14.8 MBq/kg (0.4 mCi/kg) 90Y-ibritumomab tiuxetan ("Zevalin") in elderly patients with diffuse large B-cell lymphoma and FDG-PET positive partial remission f... | |||||||||||||
Medical condition: patients with diffuse Large B-Cell lymphoma, CD20-positive | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2004-001117-34 | Sponsor Protocol Number: APL-B-013-02 | Start Date*: 2004-10-13 |
Sponsor Name:Pharma Mar S.A. | ||
Full Title: A Phase II Multicenter,Open-Label, Clinical And Pharmacokinetic Study Of Aplidin® As A 1-Hour Weekly IV Infusion, In Patients With Relapsed Or Refractory aggressive non-Hodgkin’s Lymphoma. | ||
Medical condition: Aggressive non-Hodgkin’s Lymphoma.For aggressive NHL patient cure is still the target of therapy and a CR is a prerequisite to achieve this goal. Salvage therapy needs more aggressive experimental ... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: ES (Completed) IT (Completed) | ||
Trial results: View results |
EudraCT Number: 2007-005245-37 | Sponsor Protocol Number: M06-880 | Start Date*: 2008-04-17 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Sponsor Name:Abbott GmbH & Co. KG | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Full Title: An Open-Label, Randomized, Phase 2 Study of Efficacy and Tolerability of ABT-869 in Advanced or Metastatic Non-small Cell Lung Cancer (NSCLC) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Medical condition: Advanced or Metastatic Non-small Cell Lung Cancer (NSCLC) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Trial protocol: FR (Completed) SE (Prematurely Ended) GB (Prematurely Ended) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2021-002173-26 | Sponsor Protocol Number: VX21-CTX001-151 | 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 Severe Sickle Cell Disease | |||||||||||||
Medical condition: Severe Sickle Cell Disease (SCD) | |||||||||||||
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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: 2004-004722-27 | Sponsor Protocol Number: ICT-BEM-2004-01 | Start Date*: 2005-05-12 | |||||||||||
Sponsor Name:Instituto Científico y Tecnológico de Navarra, S.A. | |||||||||||||
Full Title: Randomised, open, multicenter, sequential trial assessing the safety and efficacy of bemiparin on the response to the treatment in patients diagnosed with localized small cell carcinoma of the lung. | |||||||||||||
Medical condition: Small cell carcionoma of the lung medDRA CLASSIFICATION CODE: PT 10041071 | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-007434-20 | Sponsor Protocol Number: RV0272 | Start Date*: 2008-03-19 | |||||||||||
Sponsor Name:Deptartment of Hematology, Karolinska University Hospital | |||||||||||||
Full Title: Phase I (II) study of the combination of lenalidomide and alemtuzumab in patients with chemotherapy refractory chronic lymphocytic leukemia (CLL) | |||||||||||||
Medical condition: Refractory or relapsed chronic lymphocytic leukemia (CLL) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2016-002101-19 | Sponsor Protocol Number: CACZ885X2206 | Start Date*: 2016-11-22 | |||||||||||
Sponsor Name:Novartis Pharma Services AG | |||||||||||||
Full Title: A multiple-dose, subject- and investigator-blinded, placebo-controlled, parallel design study to assess the efficacy, safety and tolerability of ACZ885 (canakinumab) in pediatric and young adult pa... | |||||||||||||
Medical condition: Sickle cell anemia | |||||||||||||
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Population Age: Children, Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Prematurely Ended) DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-017093-20 | Sponsor Protocol Number: INT 70/09 | Start Date*: 2010-01-25 | |||||||||||
Sponsor Name:ISTITUTO NAZIONALE PER LA CURA TUMORI | |||||||||||||
Full Title: Phase 2 study with the multi-targeted tyrosine-kinase inhibitor Pazopanib (GW786034) for patients with relapsed or refractory urothelial cancer | |||||||||||||
Medical condition: Urothelial cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-004851-39 | Sponsor Protocol Number: 109/2006/U/Sper | Start Date*: 2006-10-03 | |||||||||||
Sponsor Name:AZIENDA OSPEDALIERA DI BOLOGNA POLICLINICO S. ORSOLA M. MALPIGHI | |||||||||||||
Full Title: A PHASE II, OPEN-LABEL, PROSPECTIVE, MULTICENTER STUDY TO EVALUATE THE EFFICACY AND SAFETY OF SUBSEQUENT TREATMENT WITH THE ZEVALIN (IBRITUMOMAB TIUXETAN) IN ELDERLY ( 60 YEARS) PATIENTS WITH DI... | |||||||||||||
Medical condition: DIFFUSE LARGE BCELL LYMPHOMA | |||||||||||||
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Population Age: Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-006566-42 | Sponsor Protocol Number: SIRN | Start Date*: 2007-09-03 | |||||||||||||||||||||
Sponsor Name:Universität Mainz, III. Medizinische Klinik | |||||||||||||||||||||||
Full Title: Sorafenib in Resected NSCLC (SIRN) - A Phase II Study to Investigate the Efficacy and Safety of Sorafenib as Adjuvant Treatment following Resection of Non-small Cell Lung Carcinoma (NSCLC) in Patie... | |||||||||||||||||||||||
Medical condition: Patients with histologically confirmed diagnosis of NSCLC pathological stages I, II or III A. Patients must have completely resected disease and may not be treated with prior chemotherapy. Patients... | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: DE (Prematurely Ended) | |||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2016-001058-16 | Sponsor Protocol Number: NLG-LBC-07 | Start Date*: 2017-02-15 | |||||||||||
Sponsor Name:Nordic Lymphoma Group | |||||||||||||
Full Title: A Phase II Trial of Idelalisib in Patients with Relapsed/Refractory Diffuse Large B-cell Lymphoma. | |||||||||||||
Medical condition: Relapsed/refractory diffuse large B-cell lymphoma, including transformed low grade lymphoma. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Completed) DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-016378-34 | Sponsor Protocol Number: MI-CP204 | Start Date*: 2010-06-30 | |||||||||||||||||||||
Sponsor Name:MedImmune LLC | |||||||||||||||||||||||
Full Title: An Open Label, Phase 1/2 Study of MEDI-551, a Humanized Monoclonal Antibody Directed Against CD19, in Adult Subjects With Relapsed or Refractory Advanced B-Cell Malignancies | |||||||||||||||||||||||
Medical condition: Relapsed or refractory advanced B-cell malignancies: chronic lymphocytic leukemia (CLL), small lymphocytic lymphoma (SLL), B-cell non-Hodgkin’s lymphoma (NHL) (subtypes: follicular lymphoma (FL)... | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: BE (Completed) FR (Completed) | |||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2008-000498-40 | Sponsor Protocol Number: CRAD001N2301 | Start Date*: 2009-06-08 | |||||||||||
Sponsor Name:Novartis Pharma Services AG | |||||||||||||
Full Title: A randomized, double-blind, placebo-controlled, multicenter phase III study of RAD001 adjuvant therapy in poor risk patients with Diffuse Large B-Cell Lymphoma (DLBCL) of RAD001 versus matching pla... | |||||||||||||
Medical condition: Diffuse Large B-Cell Lymphoma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: CZ (Completed) HU (Completed) SK (Completed) AT (Completed) IT (Completed) DE (Completed) GR (Completed) ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-023869-21 | Sponsor Protocol Number: ML25575 | Start Date*: 2011-02-09 | ||||||||||||||||
Sponsor Name:Roche Oy | ||||||||||||||||||
Full Title: A study of erlotinib (Tarceva®) treatment in patients with locally advanced or metastatic non-small cell lunf cancer who present activating mutations in the tyrosine kinase domain of the epidermal ... | ||||||||||||||||||
Medical condition: Locally advanced or metastatic non-small cell lung cancer with activating mutations in the tyrosine kinase domain of the epidermal growth factor receptor. | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: FI (Prematurely Ended) | ||||||||||||||||||
Trial results: View results |
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