- Trials with a EudraCT protocol (197)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
197 result(s) found for: genentech.
Displaying page 4 of 10.
| EudraCT Number: 2014-000563-41 | Sponsor Protocol Number: IMIMFTCL/GH/4 | Start Date*: 2014-08-08 |
| Sponsor Name:Consorci Mar Parc de Salut de Barcelona (Parc de Salut Mar) | ||
| Full Title: Recombinant hGH Biomarkers Discovery | ||
| Medical condition: Healthy volunteers. There is not intended indication. | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: ES (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2014-002238-29 | Sponsor Protocol Number: NL49479.029.14 | Start Date*: 2014-12-18 |
| Sponsor Name: | ||
| Full Title: Paclitaxel-trastuzumab in EGFR-mutated NSCLC patients after progression on TKI-treatment; a pilot study | ||
| Medical condition: NSCLC with EGFR mutation | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: NL (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2005-001316-47 | Sponsor Protocol Number: ML18580 | Start Date*: 2005-07-05 |
| Sponsor Name:Turku University Central Hospital | ||
| Full Title: Bevacizumab (Avastin™), dacarbazine and interferon α-2a (Roferon-A; IFN α-2a ) combination as a first-line therapy in patients with locally advancing or metastatic melanoma | ||
| Medical condition: Patients with histologically confirmed metastatic melanoma | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: FI (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2018-001773-24 | Sponsor Protocol Number: GO40558 | Start Date*: 2019-12-05 | |||||||||||||||||||||||||||||||
| Sponsor Name:Genentech Inc. | |||||||||||||||||||||||||||||||||
| Full Title: A PHASE II, OPEN-LABEL, MULTICENTER, RANDOMIZED STUDY OF THE EFFICACY AND SAFETY OF RO7198457 IN COMBINATION WITH PEMBROLIZUMAB VERSUS PEMBROLIZUMAB IN PATIENTS WITH PREVIOUSLY UNTREATED ADVANCED M... | |||||||||||||||||||||||||||||||||
| Medical condition: Advanced melanoma | |||||||||||||||||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||||||||||||
| Trial protocol: GB (GB - no longer in EU/EEA) DE (Trial now transitioned) BE (Completed) | |||||||||||||||||||||||||||||||||
| Trial results: (No results available) | |||||||||||||||||||||||||||||||||
| EudraCT Number: 2010-020101-32 | Sponsor Protocol Number: OAM4861g | Start Date*: 2010-10-21 | |||||||||||
| Sponsor Name:GENENTECH, Inc. | |||||||||||||
| Full Title: A RANDOMIZED, PHASE II, MULTICENTER, DOUBLE-BLIND, PLACEBO-CONTROLLED STUDY EVALUATING THE SAFETY AND EFFICACY OF METMAB IN COMBINATION WITH PACLITAXEL AND BEVACIZUMAB IN PATIENTS WITH METASTATIC, ... | |||||||||||||
| Medical condition: Metastatic, triple-negative breast cancer Cáncer de mama metastásico triple negativo | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Female | ||||||||||||
| Trial protocol: ES (Completed) FR (Completed) BE (Completed) DE (Completed) GB (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2007-006093-28 | Sponsor Protocol Number: FIG-DMAE | Start Date*: 2008-02-21 | |||||||||||
| Sponsor Name:Fundación de Investigación Biomédica Hospital de Getafe | |||||||||||||
| Full Title: ENSAYO CLÍNICO, ALEATORIZADO, CONTROLADO DOBLE CIEGO, MULTICÉNTRICO PARA EVALUAR LA EFICACIA Y SEGURIDAD DEL BEVACIZUMAB (AVASTIN, Genentech, Inc.) VS RANIBIZUMAB (LUCENTIS, Genentech, Inc.) INTRA... | |||||||||||||
| Medical condition: Degeneración macular asociada a la edad tipo exudativo | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: ES (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2020-005916-23 | Sponsor Protocol Number: ML39791 | Start Date*: 2020-12-18 | ||||||||||||||||
| Sponsor Name:Genentech, Inc. | ||||||||||||||||||
| Full Title: A Phase IV, Multicenter, Single-Arm, Open-Label Study of Emicizumab Prophylaxis in Patients With Hemophilia A With or Without Inhibitors Undergoing Minor Surgical Procedures | ||||||||||||||||||
| Medical condition: Hemophilia A with or without inhibitors | ||||||||||||||||||
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| Population Age: Newborns, Infants and toddlers, Children, Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: Outside EU/EEA | ||||||||||||||||||
| Trial results: View results | ||||||||||||||||||
| EudraCT Number: 2014-005438-69 | Sponsor Protocol Number: GO29646 | Start Date*: 2015-07-10 | |||||||||||
| Sponsor Name:F. Hoffmann-La Roche Ltd. | |||||||||||||
| Full Title: AN OPEN-LABEL, MULTICENTER EXTENSION STUDY OF ONARTUZUMAB IN PATIENTS WITH SOLID TUMORS ON STUDY TREATMENT PREVIOUSLY ENROLLED IN AN F. HOFFMANN-LA ROCHE- AND/OR GENENTECH-SPONSORED STUDY | |||||||||||||
| Medical condition: Solid Tumors | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: ES (Completed) LV (Completed) IT (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2019-003518-15 | Sponsor Protocol Number: CT-P6_4.2 | Start Date*: 2020-03-10 |
| Sponsor Name:Celltrion, Inc. | ||
| Full Title: A Follow-Up Study of Long-Term Efficacy of Patients with HER2-Positive Early Breast Cancer Who Had Been Enrolled in Study CT-P6 4.2 | ||
| Medical condition: Long-term safety and efficacy of treatment with CT-P6 (Herzuma) in HER-2 positive early breast cancer patients | ||
| Disease: | ||
| Population Age: Adults | Gender: Female | |
| Trial protocol: PL (Completed) RO (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2015-004616-37 | Sponsor Protocol Number: ML29966 | Start Date*: 2016-08-03 | |||||||||||||||||||||
| Sponsor Name:GENENTECH Inc. | |||||||||||||||||||||||
| Full Title: An open-label, multicenter, biomarker study to explore the mechanism of action of ocrelizumab and B-cell biology in patients with relapsing multiple sclerosis or primary progressive multiple sclero... | |||||||||||||||||||||||
| Medical condition: Relapsing Multiple Sclerosis (RMS)/Primary Progressive Multiple Sclerosis (PPMS) | |||||||||||||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||||||||||||
| Trial protocol: SE (Completed) DE (Completed) | |||||||||||||||||||||||
| Trial results: View results | |||||||||||||||||||||||
| EudraCT Number: 2021-001970-41 | Sponsor Protocol Number: 0504-19 | Start Date*: 2022-03-18 | |||||||||||
| Sponsor Name:Intas Pharmaceuticals Ltd. | |||||||||||||
| Full Title: A Double Masked, Parallel Group, Randomized, Multicenter, Clinical Study to Compare Efficacy and Safety of Intas Ranibizumab with Lucentis® in Patients with Neovascular (Wet) Age-Related Macular De... | |||||||||||||
| Medical condition: Neovascular (Wet) Age-Related Macular Degeneration (AMD) | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: CZ (Completed) HU (Completed) PL (Completed) LV (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2021-004390-31 | Sponsor Protocol Number: BP43464 | Start Date*: 2022-06-06 | |||||||||||
| Sponsor Name:F. Hoffmann-La Roche Ltd | |||||||||||||
| Full Title: A PHASE II, MULTICENTER, RANDOMIZED, DOUBLE MASKED, ACTIVE COMPARATORCONTROLLED STUDY TO INVESTIGATE THE EFFICACY, SAFETY, TOLERABILITY, PHARMACOKINETICS, AND PHARMACODYNAMICS OF RO7200220 IN COMBI... | |||||||||||||
| Medical condition: Diabetic Macular Edema (DME) | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: PL (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2011-005547-27 | Sponsor Protocol Number: GO28074 | Start Date*: 2012-10-24 | |||||||||||||||||||||
| Sponsor Name:Genentech, Inc. | |||||||||||||||||||||||
| Full Title: A PHASE II, MULTICENTER, OPEN-LABEL, RANDOMIZED STUDY EVALUATING THE EFFICACY AND SAFETY OF FOLFIRI + MEHD7945A VERSUS FOLFIRI + CETUXIMAB IN SECOND LINE IN PATIENTS WITH KRAS WILD-TYPE METASTATIC ... | |||||||||||||||||||||||
| Medical condition: Colorectal cancer that does not carry mutation in the KRAS gene | |||||||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
| Trial protocol: DE (Prematurely Ended) GB (Prematurely Ended) BE (Completed) ES (Prematurely Ended) IT (Prematurely Ended) | |||||||||||||||||||||||
| Trial results: View results | |||||||||||||||||||||||
| EudraCT Number: 2011-005539-22 | Sponsor Protocol Number: GO28076 | Start Date*: 2012-10-08 | ||||||||||||||||||||||||||
| Sponsor Name:Genentech, Inc. | ||||||||||||||||||||||||||||
| Full Title: A PHASE II, OPEN-LABEL, RANDOMIZED STUDY OF MEHD7945A VERSUS CETUXIMAB IN PATIENTS WITH RECURRENT/METASTATIC SQUAMOUS CELL CARCINOMA OF THE HEAD AND NECK WHO HAVE PROGRESSED DURING OR FOLLOWING PLA... | ||||||||||||||||||||||||||||
| Medical condition: Head and neck cancer of squamous cell origin | ||||||||||||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
| Trial protocol: BE (Completed) DE (Completed) GB (Completed) ES (Completed) HU (Completed) IT (Completed) BG (Completed) | ||||||||||||||||||||||||||||
| Trial results: View results | ||||||||||||||||||||||||||||
| EudraCT Number: 2011-000509-29 | Sponsor Protocol Number: BO25734/TDM4997g | Start Date*: 2011-12-02 | ||||||||||||||||
| Sponsor Name:F. Hoffmann-La Roche Ltd | ||||||||||||||||||
| Full Title: A Phase III randomized, multicenter, two-arm, open-label trial to evaluate the efficacy of trastuzumab emtansine compared with treatment of physician’s choice in patients with HER2-positive metasta... | ||||||||||||||||||
| Medical condition: HER2-Positive Metastatic Breast Cancer (MBC) | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: GB (Completed) SE (Completed) DE (Completed) SK (Completed) BE (Completed) CZ (Completed) HU (Completed) NO (Completed) IT (Completed) ES (Completed) | ||||||||||||||||||
| Trial results: View results | ||||||||||||||||||
| EudraCT Number: 2016-001039-11 | Sponsor Protocol Number: GA30044 | Start Date*: 2016-11-16 | |||||||||||
| Sponsor Name:Genentech, Inc. | |||||||||||||
| Full Title: A PHASE II, RANDOMIZED, DOUBLE-BLIND, PLACEBO-CONTROLLED STUDY OF THE SAFETY AND EFFICACY OF GDC-0853 IN PATIENTS WITH MODERATE TO SEVERE ACTIVE SYSTEMIC LUPUS ERYTHEMATOSUS | |||||||||||||
| Medical condition: Systemic Lupus Erythematosus | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (Completed) PT (Completed) ES (Completed) BG (Completed) DE (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2011-003720-12 | Sponsor Protocol Number: GO27820 | Start Date*: 2012-06-21 | |||||||||||||||||||||
| Sponsor Name:F. Hoffmann-La Roche Ltd. | |||||||||||||||||||||||
| Full Title: A RANDOMIZED, PHASE II, MULTICENTER, DOUBLE-BLIND, PLACEBO-CONTROLLED STUDY EVALUATING THE EFFICACY AND SAFETY OF MetMAb IN COMBINATION WITH PACLITAXEL + CISPLATIN OR CARBOPLATIN AS FIRST-LINE TREA... | |||||||||||||||||||||||
| Medical condition: MET DIAGNOSTIC−POSITIVE NON−SMALL CELL LUNG CANCER (NSCLC) | |||||||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
| Trial protocol: DE (Completed) GB (Completed) LV (Completed) ES (Completed) IT (Completed) | |||||||||||||||||||||||
| Trial results: View results | |||||||||||||||||||||||
| EudraCT Number: 2014-003231-19 | Sponsor Protocol Number: GO29294 | Start Date*: 2015-01-19 | |||||||||||
| Sponsor Name:F. Hoffmann-La Roche Ltd | |||||||||||||
| Full Title: A PHASE III, OPEN-LABEL, MULTICENTER, RANDOMIZED STUDY TO INVESTIGATE THE EFFICACY AND SAFETY OF ATEZOLIZUMAB (ANTI−PD-L1 ANTIBODY) COMPARED WITH CHEMOTHERAPY IN PATIENTS WITH LOCALLY ADVANCED OR M... | |||||||||||||
| Medical condition: Advanced tumor and metastastic disease | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: CZ (Completed) IT (Completed) PL (Completed) SI (Completed) SE (Completed) DE (Completed) GB (Completed) HU (Completed) PT (Completed) NL (Completed) FI (Completed) NO (Completed) DK (Completed) BE (Completed) AT (Completed) ES (Completed) FR (Completed) GR (Completed) RO (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2014-005490-37 | Sponsor Protocol Number: WO29522 | Start Date*: 2015-06-11 | |||||||||||
| Sponsor Name:F. Hoffmann-La Roche Ltd | |||||||||||||
| Full Title: A PHASE III, MULTICENTER, RANDOMIZED, PLACEBO-CONTROLLED STUDY OF ATEZOLIZUMAB (ANTI−PD-L1 ANTIBODY) IN COMBINATION WITH NAB-PACLITAXEL COMPARED WITH PLACEBO WITH NAB-PACLITAXEL FOR PATIENTS WITH P... | |||||||||||||
| Medical condition: Previously untreated metastatic triple negative breast cancer | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Completed) BE (Completed) GB (GB - no longer in EU/EEA) GR (Completed) ES (Ongoing) SE (Completed) DK (Prematurely Ended) LV (Completed) AT (Completed) FI (Completed) CZ (Completed) HU (Completed) PL (Completed) EE (Completed) SI (Completed) FR (Completed) RO (Completed) IT (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2011-000493-56 | Sponsor Protocol Number: PIM4973g | Start Date*: 2011-09-15 | |||||||||||||||||||||
| Sponsor Name:GENENTECH, Inc. | |||||||||||||||||||||||
| Full Title: A PHASE II, OPEN-LABEL, RANDOMIZED STUDY OF GDC-0980 VERSUS EVEROLIMUS IN PATIENTS WITH METASTATIC RENAL CELL CARCINOMA WHO HAVE PROGRESSED ON OR FOLLOWING VEGF-TARGETED THERAPY | |||||||||||||||||||||||
| Medical condition: METASTATIC RENAL CELL CARCINOMA | |||||||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
| Trial protocol: ES (Completed) DE (Completed) GB (Completed) | |||||||||||||||||||||||
| Trial results: View results | |||||||||||||||||||||||
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