- Trials with a EudraCT protocol (175)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
175 result(s) found for: Cancer AND Everolimus.
Displaying page 2 of 9.
EudraCT Number: 2013-000665-36 | Sponsor Protocol Number: UZB-MO-FC-01 | Start Date*: 2013-10-16 | |||||||||||
Sponsor Name:UZ Brussel | |||||||||||||
Full Title: A phase II, open label study of everolimus with fulvestrant in postmenopausal women with hormone receptor-positive HER-2 negative AI and fulvestrant treated, locally advanced or metastatic breast c... | |||||||||||||
Medical condition: postmenopausal women with hormone receptor-positive, Her2 negative AI and fulvestrant treated, locally advanced or metastatic breast cancer, who progressed on prior fulvestrant and also received pr... | |||||||||||||
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Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: BE (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-002872-17 | Sponsor Protocol Number: CSOM230DIC03 | Start Date*: 2013-06-24 | ||||||||||||||||
Sponsor Name:Novartis Pharma Services AG | ||||||||||||||||||
Full Title: Multicenter 3-arm trial to evaluate the efficacy and safety of Pasireotide LAR or Everolimus alone or in combination in patients with well differentiated neuroendocrine carcinoma of the lung and th... | ||||||||||||||||||
Medical condition: Neouroendocrine carcinoma of the lung and thymus | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: GB (Completed) IT (Prematurely Ended) SE (Prematurely Ended) ES (Completed) FR (Prematurely Ended) NL (Prematurely Ended) DK (Completed) DE (Prematurely Ended) GR (Prematurely Ended) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2012-000769-19 | Sponsor Protocol Number: CBEZ235Z2401 | Start Date*: 2012-10-25 | |||||||||||
Sponsor Name:Novartis Farmacéutica, S.A | |||||||||||||
Full Title: Randomized phase II study of BEZ235 or everolimus in advanced pancreatic neuroendocrine tumors | |||||||||||||
Medical condition: Adult patient in advanced pancreatic neuroendocrine tumors | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Prematurely Ended) GB (Completed) IT (Completed) FR (Completed) NL (Completed) PL (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-004120-11 | Sponsor Protocol Number: BOOG2013-06 | Start Date*: 2014-03-17 |
Sponsor Name:VU University Medical Center | ||
Full Title: PI3K pathway analysis in tumor tissue and circulating DNA to obtain further insight in the efficacy of everolimus when combined with exemestane. A side-study protocol attached to standard treatmen... | ||
Medical condition: Hormone receptor-positive advanced metastatic breast cancer in postmenopausal patients who have progressed on anastrozole or letrozole. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2007-001951-20 | Sponsor Protocol Number: UCL/06/053 | Start Date*: 2008-03-12 | ||||||||||||||||
Sponsor Name:University College London | ||||||||||||||||||
Full Title: A phase I and randomised phase II study of Docetaxel and RAD001 (Everolimus) in advanced/recurrent or metastatic squamous cell carcinoma of the head and neck | ||||||||||||||||||
Medical condition: Locally advanced or metastatic squamous cell carcinoma of the head and neck | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: GB (Prematurely Ended) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2011-005132-26 | Sponsor Protocol Number: CA209-025 | Start Date*: 2012-09-11 | |||||||||||||||||||||
Sponsor Name:Bristol-Myers Squibb International Corporation | |||||||||||||||||||||||
Full Title: A Randomized, Open-Label, Phase 3 Study of Nivolumab (BMS-936558) vs. Everolimus in Subjects with Advanced or Metastatic Clear-Cell Renal Cell Carcinoma Who Have Received Prior Anti-Angiogenic Ther... | |||||||||||||||||||||||
Medical condition: Advanced or metastatic (medically or surgically unresectable) clear-cell Renal Cell Carcinoma | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: IE (Completed) SE (Completed) GB (GB - no longer in EU/EEA) FI (Completed) BE (Completed) DE (Completed) IT (Completed) AT (Completed) HU (Completed) CZ (Completed) DK (Completed) ES (Completed) NO (Completed) GR (Completed) | |||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2016-000916-14 | Sponsor Protocol Number: E7080-G000-307 | Start Date*: 2017-07-19 | |||||||||||
Sponsor Name:Eisai Ltd. | |||||||||||||
Full Title: A Multicenter, Open-label, Randomized, Phase 3 Trial to Compare the Efficacy and Safety of Lenvatinib in Combination with Everolimus or Pembrolizumab Versus Sunitinib Alone in First-Line Treatment ... | |||||||||||||
Medical condition: Advanced Renal Cell Carcinoma | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) GB (GB - no longer in EU/EEA) CZ (Completed) IE (Completed) AT (Completed) BE (Completed) ES (Completed) PL (Completed) GR (Completed) NL (Completed) IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2022-000199-20 | Sponsor Protocol Number: ML43171 | Start Date*: 2022-07-27 | ||||||||||||||||||||||||||
Sponsor Name:Genentech, Inc. | ||||||||||||||||||||||||||||
Full Title: A PHASE III RANDOMIZED, OPEN-LABEL, MULTICENTER STUDY EVALUATING THE EFFICACY AND SAFETY OF GIREDESTRANT PLUS EVEROLIMUS COMPARED WITH EXEMESTANE PLUS EVEROLIMUS IN PATIENTS WITH ESTROGEN RECEPTOR-... | ||||||||||||||||||||||||||||
Medical condition: Estrogen Receptor (ER)-Positive, HER2-Negative, Locally Advanced or Metastatic Breast Cancer previously treated with a CDK4/6 inhibitor and endocrine therapy | ||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: ES (Ongoing) IT (Trial now transitioned) GR (Trial now transitioned) | ||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2014-003951-72 | Sponsor Protocol Number: GOIRC02/2014 | Start Date*: 2015-03-05 |
Sponsor Name:Gruppo Oncologico Italiano Ricerca Cancro (GOIRC) | ||
Full Title: Phase II randomized multicenter study of Everolimus as maintenance therapy for metastatic neuroendocrine carcinoma with pulmonary or gastroenteropancreatic origin. | ||
Medical condition: The aim of this study is to evaluate the activity of a maintenance therapy with everolimus 10 mg daily in patients with stable disease, partial response or complete response after 6 cycles of indu... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: IT (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2013-000726-66 | Sponsor Protocol Number: GETNE1206 | Start Date*: 2014-10-08 | ||||||||||||||||
Sponsor Name:Grupo Español de Tumores Neuroendocrinos (GETNE) | ||||||||||||||||||
Full Title: Randomized open label study to compare the efficacy and safety of everolimus followed by chemotherapy with STZ-5FU upon progression or the reverse sequence, chemotherapy with STZ-5FU followed by ... | ||||||||||||||||||
Medical condition: advanced progressive pNETs | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: SE (Completed) DE (Completed) IT (Completed) ES (Completed) DK (Completed) NL (Completed) FR (Completed) GB (GB - no longer in EU/EEA) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2014-002114-23 | Sponsor Protocol Number: BAY88-8223/17096 | Start Date*: 2015-10-26 | |||||||||||
Sponsor Name:Bayer HealthCare AG | |||||||||||||
Full Title: A phase II randomized, double-blind, placebo-controlled trial of radium-223 dichloride in combination with exemestane and everolimus versus placebo in combination with exemestane and everolimus whe... | |||||||||||||
Medical condition: Metastatic HER2 negative hormone receptor positive breast cancer subjects with bone metastases | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: IT (Completed) GB (Completed) ES (Completed) AT (Completed) CZ (Completed) NL (Completed) DE (Completed) BE (Completed) FR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-004035-38 | Sponsor Protocol Number: GIM16-FEVEX | Start Date*: 2015-06-17 | |||||||||||
Sponsor Name:CONSORZIO ONCOTECH | |||||||||||||
Full Title: Fulvestrant ed EVerolimus più EXemestane nel carcinoma mammario metastatico” “Fulvestrant followed by everolimus plus exemestane vs examestane and everolimus followed by fulvestrant in postmenopaus... | |||||||||||||
Medical condition: Hormone receptor positive (HR+) and human epidermal growth factor receptor type 2 negative (HER2-) locally advanced (LABC) or metastatic breast cancer (MBC) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2010-023183-40 | Sponsor Protocol Number: CSOM230I2201 | Start Date*: 2011-06-28 | |||||||||||
Sponsor Name:Novartis Pharma Services AG | |||||||||||||
Full Title: A randomized, open-label phase II multicenter study evaluating the efficacy of oral Everolimus alone or in combination with Pasireotide LAR i.m. in advanced progressive pancreatic neuroendocrine tu... | |||||||||||||
Medical condition: advanced progressive pancreatic neuroendocrine tumors (PNET) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Prematurely Ended) SE (Prematurely Ended) BE (Completed) DK (Prematurely Ended) DE (Completed) HU (Completed) ES (Completed) NL (Prematurely Ended) IT (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-001110-15 | Sponsor Protocol Number: 1280.4 | Start Date*: 2014-04-25 | |||||||||||
Sponsor Name:Boehringer Ingelheim España, S.A. | |||||||||||||
Full Title: A Phase Ib/II Randomized Study of BI 836845 in Combination with Exemestane and Everolimus Versus Exemestane and Everolimus Alone in Women with Locally Advanced or Metastatic Breast Cancer | |||||||||||||
Medical condition: Locally Advanced or Metastatic Breast Cancer positive for estrogen-receptor (ER) and/or progesterone receptor (PgR) and negative for HER2 which is refractory to non-steroidal aromatase inhibitor (... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: ES (Completed) FR (Completed) BE (Completed) NL (Completed) SE (Completed) IE (Completed) AT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-002524-16 | Sponsor Protocol Number: 240562-2013-01 | Start Date*: 2014-01-10 |
Sponsor Name:Dept of Oncology. Haukeland University Hospital | ||
Full Title: Everolimus and temozolomide as first-line treatment in advanced gastrointestinal neuroendocrine carcinoma (G3) with a Ki67 of 20-55% | ||
Medical condition: Everolimus and temozolomide as first-line treatment in advanced gastrointestinal neuroendocrine carcinoma (G3) with a Ki67 of 20-55% | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: SE (Completed) DK (Completed) | ||
Trial results: View results |
EudraCT Number: 2019-003444-72 | Sponsor Protocol Number: MK-6482-005 | Start Date*: 2020-02-17 | |||||||||||
Sponsor Name:Merck Sharp & Dohme LLC | |||||||||||||
Full Title: An Open-label, Randomized Phase 3 Study of MK-6482 Versus Everolimus in Participants with Advanced Renal Cell Carcinoma That Has Progressed After Prior PD- 1/L1 and VEGF-Targeted Therapies | |||||||||||||
Medical condition: Advanced Renal Cell Carcinoma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FI (Trial now transitioned) NO (Trial now transitioned) HU (Trial now transitioned) DE (Trial now transitioned) FR (Trial now transitioned) DK (Trial now transitioned) ES (Ongoing) GB (GB - no longer in EU/EEA) SE (Trial now transitioned) IT (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-000127-32 | Sponsor Protocol Number: ROPETAR | Start Date*: 2011-11-03 | |||||||||||||||||||||
Sponsor Name:Werkgroep Immunotherapie Nederland voor Oncologie | |||||||||||||||||||||||
Full Title: A randomized phase II study to explore the efficacy and feasibility of upfront bi-monthly rotations between Everolimus and Pazopanib with sequential treatment of first line Pazopanib and second lin... | |||||||||||||||||||||||
Medical condition: Advanced or metastatic clear cell renal cancer. | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: NL (Completed) | |||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2008-008697-31 | Sponsor Protocol Number: CRAD001W2301 | Start Date*: 2009-11-12 | |||||||||||
Sponsor Name:Novartis Pharma Services AG | |||||||||||||
Full Title: A randomized Phase III, double-blind, placebo-controlled multicenter trial of daily everolimus in combination with trastuzumab and vinorelbine, in pretreated women with HER2/neu over-expressing loc... | |||||||||||||
Medical condition: HER2-neu overexpressing metastatic breast cancer after previous trastuzumab use | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: DE (Completed) GR (Completed) BE (Completed) IT (Completed) ES (Completed) FR (Completed) CZ (Completed) GB (Completed) HU (Completed) SK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-001010-14 | Sponsor Protocol Number: XL184-308 | Start Date*: 2013-08-15 | |||||||||||
Sponsor Name:Exelixis, Inc. | |||||||||||||
Full Title: A Phase 3, Randomized, Controlled Study of Cabozantinib (XL184) vs Everolimus in Subjects with Metastatic Renal Cell Carcinoma that has Progressed after Prior VEGFR Tyrosine Kinase Inhibitor Therapy | |||||||||||||
Medical condition: Metastatic renal cell carcinoma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: HU (Completed) AT (Completed) SE (Completed) BE (Completed) CZ (Completed) PT (Completed) IE (Completed) IT (Completed) NL (Completed) SK (Completed) GB (Completed) ES (Completed) DE (Completed) DK (Completed) FR (Completed) FI (Completed) PL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2016-002778-11 | Sponsor Protocol Number: E7080-G000-218 | Start Date*: 2017-06-12 | ||||||||||||||||
Sponsor Name:Eisai Ltd | ||||||||||||||||||
Full Title: A Randomized, Open-label (formerly Double-blind), Phase 2 Trial to Assess Safety and Efficacy of Lenvatinib at Two Different Starting Doses (18 mg vs. 14 mg QD) in Combination with Everolimus (5 mg... | ||||||||||||||||||
Medical condition: Advanced renal cell carcinoma | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: CZ (Completed) GB (GB - no longer in EU/EEA) NL (Completed) GR (Completed) FI (Completed) PL (Completed) ES (Ongoing) PT (Completed) IT (Completed) RO (Ongoing) | ||||||||||||||||||
Trial results: View results |
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