- Trials with a EudraCT protocol (3,871)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
3,871 result(s) found for: Cell function.
Displaying page 1 of 194.
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: 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: 2011-001791-19 | Sponsor Protocol Number: G300504 | Start Date*: 2011-09-22 | |||||||||||||||||||||
Sponsor Name:GTx, Inc. | |||||||||||||||||||||||
Full Title: Phase III, Randomized, Double-Blind, Placebo-Controlled Study of the Effect of GTx-024 on Muscle Wasting in Patients with Non-Small Cell Lung Cancer on First Line Platinum Plus a Taxane Chemotherapy | |||||||||||||||||||||||
Medical condition: Cachexia, muscle wasting in patients with Non-Small Cell Lung Cancer | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: HU (Completed) | |||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-007696-16 | Sponsor Protocol Number: TOGA 0601 | Start Date*: 2008-06-02 | ||||||||||||||||
Sponsor Name:TOGA Thoracic Oncology Group Antwerp | ||||||||||||||||||
Full Title: Low molecular weight heparin in advanced non small cell lung cancer (NSCLC): a randomized open label phase III study evaluating the effect of enoxaparin (Clexane) on survival and symptom control in... | ||||||||||||||||||
Medical condition: Non Small Cell Lung Cancer | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: BE (Prematurely Ended) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-000570-22 | Sponsor Protocol Number: 20060441 | Start Date*: 2008-01-07 | ||||||||||||||||||||||||||
Sponsor Name:Amgen Inc | ||||||||||||||||||||||||||||
Full Title: A Randomized, Double-Blind, Trial of AMG 745 or Placebo for the Treatment of Cachexia in Subjects with Non-Small Cell Lung Cancer | ||||||||||||||||||||||||||||
Medical condition: Muscle cachexia due to non-small cell lung cancer (NSCLC). | ||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: DE (Completed) SE (Prematurely Ended) | ||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2012-000473-23 | Sponsor Protocol Number: RETRY | Start Date*: 2012-05-29 | |||||||||||
Sponsor Name:GIOM - Gruppo Italiano Oncologia Nefrologica | |||||||||||||
Full Title: PHASE II STUDY OF SUNITINIB AS RECHALLENGE THIRD-LINE THERAPY IN METASTATIC RENAL CANCER | |||||||||||||
Medical condition: Metastatic renal cancer thrid-line therapy already treated in fist-line therapy with Sunitinib. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-003690-40 | Sponsor Protocol Number: 944/08 | Start Date*: 2008-06-16 | |||||||||||
Sponsor Name:POLICLINICO UNIVERSITARIO AGOSTINO GEMELLI | |||||||||||||
Full Title: Low-doses radiotherapy and concomitant chemotherapy with pemetrexed in progression desease NSCLC: a dose-descalation phase II study | |||||||||||||
Medical condition: advanced and/or metastatic NSCLC | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
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: 2012-001337-13 | Sponsor Protocol Number: CRAD001LIC34T | Start Date*: 2012-08-17 | |||||||||||
Sponsor Name:APRO | |||||||||||||
Full Title: A randomized phase II study to explore the efficacy and feasibility of upfront rotations between sunitinib and everolimus versus sequential treatment of first line sunitinib and second line everoli... | |||||||||||||
Medical condition: Metastatic clear cell renal cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) GR (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2016-002552-24 | Sponsor Protocol Number: PKAPIR | Start Date*: 2016-12-16 | |||||||||||
Sponsor Name:Centre Georges François Leclerc | |||||||||||||
Full Title: Pemetrexed (Alimta®) in maintenance in patients with impaired renal function: multicenter randomized Phase 4 study comparing two strategies for dose calculation | |||||||||||||
Medical condition: Patients with non-small lung cell cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2018-003608-38 | Sponsor Protocol Number: CSEG101A2203 | Start Date*: 2019-12-04 | ||||||||||||||||
Sponsor Name:Novartis Pharma AG | ||||||||||||||||||
Full Title: A Phase II, multicenter, randomized, open label two arm study comparing the effect of crizanlizumab + standard of care to standard of care alone on renal function in sickle cell disease patients ≥ ... | ||||||||||||||||||
Medical condition: Sickle Cell Disease; Sickle Cell Nephropathy | ||||||||||||||||||
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Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) GR (Completed) ES (Ongoing) FR (Completed) IT (Prematurely Ended) NL (Completed) IE (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2021-005136-34 | Sponsor Protocol Number: THIO101 | Start Date*: 2022-11-16 | |||||||||||||||||||||
Sponsor Name:MAIA Biotechnology, Inc. | |||||||||||||||||||||||
Full Title: A Multicenter, Open-Label, Dose-Finding, Phase 2 Study Evaluating THIO Sequenced with Cemiplimab (LIBTAYO®) in Subjects with Advanced Non-Small Cell Lung Cancer (NSCLC) | |||||||||||||||||||||||
Medical condition: Non-Small Cell Lung Cancer | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: BG (Trial now transitioned) PL (Trial now transitioned) | |||||||||||||||||||||||
Trial results: (No results available) |
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: 2022-002226-27 | Sponsor Protocol Number: HLX10-020-SCLC302 | Start Date*: 2022-11-17 | |||||||||||
Sponsor Name:Shanghai Henlius Biotech, Inc. | |||||||||||||
Full Title: A Randomized, Double-Blind, International Multicenter, Phase III Study to Evaluate the Anti-Tumor Efficacy and Safety of HLX10 (Recombinant Humanized Anti-PD-1 Monoclonal Antibody Injection) or Pla... | |||||||||||||
Medical condition: Patients with Limited-Stage Small Cell Lung Cancer (LS-SCLC) at stage I-III of the AJCC 8th edition of the cancer staging | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Ongoing) DE (Trial now transitioned) HU (Trial now transitioned) PL (Trial now transitioned) AT (Trial now transitioned) LV (Trial now transitioned) CZ (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
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: 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 |
EudraCT Number: 2006-003298-28 | Sponsor Protocol Number: M06-822 | Start Date*: 2007-05-23 | |||||||||||
Sponsor Name:Abbott Laboratories Limited (Queenborough, Kent, ME11 5EL, England) | |||||||||||||
Full Title: A Phase 1/2a Study Evaluating the Safety, Pharmacokinetics, and Efficacy of ABT-263 in Subjects with Small Cell Lung Cancer (SCLC) or other non-hematological malignancies. | |||||||||||||
Medical condition: Small cell lung carcinoma (SCLC) (North America or UK) and other non-hematological malignancies (North America only). | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-005520-16 | Sponsor Protocol Number: BO20603 | Start Date*: 2007-05-02 | |||||||||||
Sponsor Name:F. Hoffmann-La Roche Ltd | |||||||||||||
Full Title: Ensayo clínico de fase III multicéntrico, randomizado, doble ciego, controlado con placebo, para comparar la eficacia de bevacizumab en combinación con rituximab y CHOP (RA CHOP) frente a rituxima... | |||||||||||||
Medical condition: Pacientes con linfoma difuso de células B grandes (LDCBG) CD20-positivo no tratados previamente, que presentan enfermedad de riesgo intermedio-bajo, intermedio-alto o alto, de acuerdo con el índic... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) AT (Completed) FR (Completed) CZ (Completed) GR (Completed) PT (Completed) GB (Completed) SE (Completed) DE (Completed) IT (Completed) PL (Completed) SK (Completed) LT (Completed) HU (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-001792-39 | Sponsor Protocol Number: G300505 | Start Date*: 2012-01-04 | |||||||||||||||||||||
Sponsor Name:GTx, Inc. | |||||||||||||||||||||||
Full Title: Phase III, Randomized, Double-Blind, Placebo-Controlled Study of the Effect of GTx-024 on Muscle Wasting in Patients with Non-Small Cell Lung Cancer on First Line Platinum Plus a Non-Taxane Chemoth... | |||||||||||||||||||||||
Medical condition: Cachexia, muscle wasting in patients with Non-Small Cell Lung Cancer | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: PL (Completed) HU (Completed) | |||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2020-005618-16 | Sponsor Protocol Number: CR187-18 | Start Date*: 2021-02-04 | ||||||||||||||||||||||||||
Sponsor Name:CuraTeQ Biologics Private Limited | ||||||||||||||||||||||||||||
Full Title: A Multicenter, Randomised, Double blind, Parallel, Phase III Global Study to Assess the Efficacy and Safety of BP01 (Bevacizumab) when compared to Avastin®-EU in Combination with Carboplatin and Pa... | ||||||||||||||||||||||||||||
Medical condition: Newly diagnosed or recurrent Stage IIIB/IV Non Squamous (ns) Non-Small Cell Lung Cancer (NSCLC). | ||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: HU (Completed) BG (Completed) | ||||||||||||||||||||||||||||
Trial results: (No results available) |
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