- Trials with a EudraCT protocol (3,190)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
3,190 result(s) found for: roche OR chugai OR genentech.
Displaying page 68 of 160.
EudraCT Number: 2005-002484-87 | Sponsor Protocol Number: GAST-TaxXel | Start Date*: 2005-07-11 |
Sponsor Name:Raija Ristamäki | ||
Full Title: Biweekly Taxotere in combination with Xeloda as first-line treatment in patients with advanced gastric cancer | ||
Medical condition: advanced gastric cancer | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: FI (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2006-005110-12 | Sponsor Protocol Number: v2bis2006-09-27 | Start Date*: 2007-03-12 |
Sponsor Name:CHU de Besançon | ||
Full Title: Evaluation de l'association Fofiri 3 et bévacizumab (Avastin) dans le traitement des cadénocarcinomes colorectaux métastasiques | ||
Medical condition: colorectal adenocarcinoma with metastases | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: FR (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2017-004606-18 | Sponsor Protocol Number: WASH-OUT | Start Date*: 2018-06-19 | |||||||||||
Sponsor Name:UNIVERSITÀ CAMPUS BIO-MEDICO DI ROMA | |||||||||||||
Full Title: Terapia di disassuefazione con metilprednisolone e diazepam ev in pazienti affetti da cefalea cronica con uso eccessivo di sintomatici | |||||||||||||
Medical condition: Emicrania Cronica e Cefalea da Iperuso di Farmaci | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2015-001072-22 | Sponsor Protocol Number: T51/2015 | Start Date*: 2016-01-26 | |||||||||||
Sponsor Name:Turku University Hospital | |||||||||||||
Full Title: Clinical and virological efficacy of pegylated interferon alpha in the treatment of rhinovirus infection in patients with primary hypogammaglobulinemia: randomized controlled trial | |||||||||||||
Medical condition: Rhinovirus infection | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FI (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2013-004303-39 | Sponsor Protocol Number: NVALT17 | Start Date*: 2014-04-11 | |||||||||||
Sponsor Name:Stichting NVALT Studies | |||||||||||||
Full Title: A randomized phase III study of erlotinib compared to intercalated erlotinib with cisplatinum pemetrexed as first-line therapy for advanced EGFR mutated non-small-cell lung cancer. The NVALT17 study | |||||||||||||
Medical condition: Advanced non-small cell lung cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Completed) BE (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2004-004545-18 | Sponsor Protocol Number: NA | Start Date*: 2005-04-26 |
Sponsor Name:CHU Sart Tilman | ||
Full Title: Cell therapy for cardiac repair through mobilization of hematopoietic stem cells and endothelial progenitors in patients with chronic ischemic cardiomyopathy. | ||
Medical condition: Chronic ischemic cardiac disease | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: BE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2014-000333-23 | Sponsor Protocol Number: RCSI/SSI/2015 | Start Date*: 2015-10-02 |
Sponsor Name:Beaumont Hospital | ||
Full Title: Alcohol-based povidone iodine versus chlorhexidine-alcohol in the prevention of surgical site infection: A prospective comparative study | ||
Medical condition: Surgical Site Infection | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: IE (Prematurely Ended) | ||
Trial results: (No results available) |
EudraCT Number: 2019-001754-25 | Sponsor Protocol Number: 371c | Start Date*: 2019-11-25 |
Sponsor Name:Reade | ||
Full Title: Using adalimumab serum concentration to choose a subsequent biological treatment in rheumatoid arthritis patients failing adalimumab treatment (ADDORA-switch): an open label randomized superiority ... | ||
Medical condition: rheumatoid arthritis | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2015-002156-27 | Sponsor Protocol Number: 1356/2015 | Start Date*: Information not available in EudraCT |
Sponsor Name:Medical University of Vienna | ||
Full Title: Prospective controlled study of reduced-dose Rituximab in rheumatoid arthritis patients in low disease activity and remission – the REDOREM study | ||
Medical condition: rheumatoid arthritis | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: AT (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2016-004529-17 | Sponsor Protocol Number: YO39609 | Start Date*: 2018-07-17 | ||||||||||||||||
Sponsor Name:F. Hoffman-La Roche Ltd | ||||||||||||||||||
Full Title: A PHASE Ib/II, OPEN-LABEL, MULTICENTER, RANDOMIZED, UMBRELLA STUDY EVALUATING THE EFFICACY AND SAFETY OF MULTIPLE IMMUNOTHERAPY-BASED TREATMENT COMBINATIONS IN PATIENTS WITH LOCALLY ADVANCED UNRESE... | ||||||||||||||||||
Medical condition: Locally advanced unresectable or Metastatic gastric or gastroesophageal junction cancer or esophageal cancer | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) ES (Prematurely Ended) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2014-005341-44 | Sponsor Protocol Number: ICT | Start Date*: 2015-05-04 |
Sponsor Name:Medical University of Graz | ||
Full Title: Molecular-biological tumor profiling for drug treatment selection in patients with advanced and refractory carcinoma | ||
Medical condition: Patients with locally advanced and/ or metastasized carcinoma for whom no further evidence-based drug treatment is established.A progression of the tumor is confirmed due to the last evidence-based... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: AT (Completed) | ||
Trial results: View results |
EudraCT Number: 2011-003617-42 | Sponsor Protocol Number: BP25466 | Start Date*: 2011-12-14 | ||||||||||||||||
Sponsor Name:F. Hoffmann-La Roche Ltd. | ||||||||||||||||||
Full Title: An adaptive, multi-center, randomized, investigator-masked, subject-masked, multiple-dose, placebo-controlled, parallel study to investigate efficacy, safety, tolerability and pharmacokinetics of... | ||||||||||||||||||
Medical condition: Primary open angle glaucoma or ocular hypertension | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: HU (Prematurely Ended) CZ (Prematurely Ended) BG (Prematurely Ended) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2011-002160-24 | Sponsor Protocol Number: BP25712 | Start Date*: 2012-04-12 | ||||||||||||||||
Sponsor Name:F. Hoffmann-La Roche Ltd. | ||||||||||||||||||
Full Title: A Multi-Center, Randomized, Double-Blind, Placebo-Controlled, Parallel-Group Study to Investigate the Efficacy and Safety of RO4995819 Versus Placebo, as Adjunctive Therapy in Patients with Major D... | ||||||||||||||||||
Medical condition: Major Depressive Disorder | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: AT (Completed) DE (Completed) SK (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2018-002964-25 | Sponsor Protocol Number: GO40800 | Start Date*: 2019-04-25 | |||||||||||
Sponsor Name:F. Hoffmann-La Roche Ltd | |||||||||||||
Full Title: A PHASE IB/II STUDY, EVALUATING THE SAFETY AND EFFICACY OF IDASANUTLIN IN COMBINATION WITH CYTARABINE AND DAUNORUBICIN IN PATIENTS NEWLY DIAGNOSED WITH ACUTE MYELOID LEUKEMIA (AML) AND THE SAFETY A... | |||||||||||||
Medical condition: Acute myeloid leukemia (AML) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Prematurely Ended) ES (Prematurely Ended) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-019912-18 | Sponsor Protocol Number: NA25220 | Start Date*: 2011-01-17 | |||||||||||
Sponsor Name:F. Hoffmann-La Roche Ltd. | |||||||||||||
Full Title: A randomized, double-blind, parallel-group study of safety and the effect on clinical outcome of tocilizumab SC versus placebo SC in combination with traditional disease modifying anti-rheumatic dr... | |||||||||||||
Medical condition: Rheumatoid arthritis (RA) Artritis Reumatoide (AR) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) GR (Completed) HU (Completed) BG (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2015-003386-28 | Sponsor Protocol Number: GH29914 | Start Date*: 2016-05-11 | |||||||||||
Sponsor Name:F. Hoffmann-La Roche Ltd | |||||||||||||
Full Title: A phase Ib/II multi-arm study with venetoclax in combination with cobimetinib, and venetoclax in combination with idasanutlin in patients ≥ 60 years with relapsed or refractory acute myeloid leukem... | |||||||||||||
Medical condition: Relapsed or Refractory Acute Myeloid Leukemia | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Prematurely Ended) IT (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2020-003515-10 | Sponsor Protocol Number: BP41783 | Start Date*: 2021-03-09 | |||||||||||
Sponsor Name:F. Hoffmann-La Roche Ltd | |||||||||||||
Full Title: A LONGITUDINAL, BIOMARKER STUDY OF ANTI-VEGF, TO EXPLORE THE RELATIONSHIP BETWEEN AQUEOUS HUMOR COMPOSITION AND MULTIMODAL RETINAL IMAGING IN NEOVASCULAR AGE-RELATED MACULAR DEGENERATION AND DIABET... | |||||||||||||
Medical condition: Treatment Naïve Neovascular Age-Related Macular Degeneration (nAMD) and Treatment Naïve diabetic macular edema (DME) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: CZ (Completed) PL (Completed) IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-004362-17 | Sponsor Protocol Number: MITO-16b/MANGO-OV2b/ENGOT-OV17 | Start Date*: 2013-01-20 | |||||||||||
Sponsor Name:ISTITUTO NAZIONALE PER LO STUDIO E LA CURA DEI TUMORI - FONDAZIONE 'G. PASCALE' | |||||||||||||
Full Title: A multicenter phase III randomized study with second line chemotherapy plus or minus bevacizumab in patients with platinum sensitive epithelial ovarian cancer recurrence after a bevacizumab/chemoth... | |||||||||||||
Medical condition: platinum sensitive ovarian cancer patients progressing or recurring after a first-line treatment including bevacizumab. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: IT (Completed) GR (Completed) FR (Ongoing) BE (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-003568-73 | Sponsor Protocol Number: GECP06/01 | Start Date*: 2008-05-07 | |||||||||||
Sponsor Name:Grupo Espagnol de Cancer de Pulmon | |||||||||||||
Full Title: Phase III, Multicenter, Open-label, Randomized Study of Erlotinib (Tarceva®) Treatment Versus Chemotherapy in Patients with Advanced Non-small-cell Carcinoma of the Lung Who Present Mutations in th... | |||||||||||||
Medical condition: Non-squamous-cell, non-small-cell lung cancer in stage IIIB and IV | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) IT (Prematurely Ended) ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-005129-31 | Sponsor Protocol Number: BH21260 | Start Date*: 2008-10-22 | |||||||||||
Sponsor Name:F.Hoffmann-La Roche Ltd | |||||||||||||
Full Title: A randomized, controlled, open-label, multi-centre, parallel-group study to assess all-cause mortality and cardiovascular morbidity in patients with chronic kidney disease on dialysis and those not... | |||||||||||||
Medical condition: To gain more experience with MIRCERA administered under clinical practice conditions and according to the approved label by performing a non-inferiority study comparing MIRCERA to other ESAs in ter... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) GB (Completed) BE (Completed) CZ (Completed) IT (Completed) SE (Completed) LT (Completed) GR (Completed) FR (Completed) | |||||||||||||
Trial results: View results |
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