- Trials with a EudraCT protocol (314)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
314 result(s) found for: Everolimus.
Displaying page 13 of 16.
EudraCT Number: 2010-019966-95 | Sponsor Protocol Number: CRAD001L2402T | Start Date*: 2011-01-13 | |||||||||||
Sponsor Name:Duke University | |||||||||||||
Full Title: A Randomized Phase II Study of Afinitor (RAD001) vs. Sutent (Sunitinib) in Patients with Metastatic Non-Clear Cell Renal Cell Carcinoma (ASPEN) | |||||||||||||
Medical condition: Histologically confirmed advanced Renal Cell Carcinoma, with non-clear cell pathology. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-016640-39 | Sponsor Protocol Number: PCLD003 | Start Date*: 2010-05-31 | ||||||||||||||||
Sponsor Name:Radboud University Nijmegen Medical Centre | ||||||||||||||||||
Full Title: Everolimus added to long acting octreotide as a volume reducing treatment of polycystic livers. | ||||||||||||||||||
Medical condition: Isolated polycystic liver disease | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: NL (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2018-003194-10 | Sponsor Protocol Number: 789456 | Start Date*: 2019-03-19 |
Sponsor Name:UMCG | ||
Full Title: OPen label multicenter randomized Trial comparing standard IMmunosuppression with tacrolimus and mycophenolate mofetil with a low exposure tacrolimus regimen In combination with everolimus in de no... | ||
Medical condition: de novo renal transplantation in elderly patients. | ||
Disease: | ||
Population Age: Elderly | Gender: Male, Female | |
Trial protocol: NL (Trial now transitioned) | ||
Trial results: (No results available) |
EudraCT Number: 2014-004557-14 | Sponsor Protocol Number: NA | Start Date*: 2015-02-09 | |||||||||||
Sponsor Name:King's College London [...] | |||||||||||||
Full Title: Prospective randomised marker-based trial to assess the clinical utility and safety of biomarker-guided immunosuppression withdrawal in liver transplantation | |||||||||||||
Medical condition: Immunosuppression withdrawal in liver transplantation | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) BE (Completed) ES (Prematurely Ended) DE (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2016-004432-38 | Sponsor Protocol Number: CINC424D2301 | Start Date*: 2017-10-11 | ||||||||||||||||||||||||||
Sponsor Name:Novartis Pharma AG | ||||||||||||||||||||||||||||
Full Title: A phase III randomized open-label multi-center study of ruxolitinib vs. best available therapy in patients with corticosteroid-refractory chronic graft versus host disease after allogeneic stem cel... | ||||||||||||||||||||||||||||
Medical condition: corticosteroid refractory chronic Graft vs Host Disease | ||||||||||||||||||||||||||||
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Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) SE (Completed) DE (Completed) AT (Completed) ES (Ongoing) BE (Completed) DK (Completed) NL (Completed) IT (Completed) FR (Completed) PT (Completed) HU (Completed) PL (Completed) BG (Completed) NO (Completed) GR (Completed) RO (Ongoing) | ||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2015-002867-41 | Sponsor Protocol Number: OPS-C-001/D-FR-01072-001 | Start Date*: 2015-12-10 | |||||||||||
Sponsor Name:Ipsen Pharma | |||||||||||||
Full Title: An international multi-center, open-label study to evaluate safety, tolerability, biodistribution, dosimetry and preliminary efficacy of 177Lu-OPS201 for the therapy of somatostatin receptor positi... | |||||||||||||
Medical condition: Neuroendocrine tumors (NETs) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: AT (Completed) GB (GB - no longer in EU/EEA) DK (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-005294-60 | Sponsor Protocol Number: CRAD001C24114 | Start Date*: Information not available in EudraCT | |||||||||||
Sponsor Name:Novartis Pharma GmbH | |||||||||||||
Full Title: Multicenter, triple-arm, single-stage, phase II trial to determine the preliminary efficacy and safety of RAD001 in patients with histological evidence of progressive or metastatic bone or soft tis... | |||||||||||||
Medical condition: histological evidence of progressive or metastatic bone or soft tissue sarcomas | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-000077-38 | Sponsor Protocol Number: CRAD001L2201 | Start Date*: 2008-10-09 | |||||||||||
Sponsor Name:Novartis Pharma Services AG | |||||||||||||
Full Title: A randomized, open label, multi-center phase II study to compare bevacizumab plus RAD001 versus interferon alfa-2a and bevacizumab for the first-line treatment of patients with metastatic clear cel... | |||||||||||||
Medical condition: Patients with metastatic clear cell carcinoma of the kidney | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SK (Completed) BE (Prematurely Ended) GB (Prematurely Ended) CZ (Prematurely Ended) HU (Prematurely Ended) ES (Prematurely Ended) DE (Completed) IT (Prematurely Ended) FR (Completed) NL (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-010640-34 | Sponsor Protocol Number: THYTOTRA | Start Date*: 2009-08-13 | |||||||||||
Sponsor Name:AZIENDA OSPEDALIERA POLICLINICO DI MODENA | |||||||||||||
Full Title: INDUCTION OF DONOR-SPECIFIC TOLERANCE IN PATIENTS WITH LIVER TRANSPLANTATION WITH RECIPIENT PRE-TREATMENT WITH THYMOGLOBULINE AND MINIMAL POST-TRANSPLANT IMMUNOSUPPRESSION. | |||||||||||||
Medical condition: Adult recipients of first liver transplantation | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
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: 2013-000819-25 | Sponsor Protocol Number: 43712 | Start Date*: 2013-10-22 |
Sponsor Name:Leiden University Medical Center | ||
Full Title: Autologous BM derived MSCs in combination with everolimus to preserve renal structure and function in renal recipients | ||
Medical condition: renal recipients | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2008-006841-25 | Sponsor Protocol Number: CRAD001CCH08t | Start Date*: 2009-08-24 | |||||||||||
Sponsor Name:Oncology Institute of Southern Switzerland | |||||||||||||
Full Title: Phase II study of the combination of RAD001 and Letrozole in patients with recurrent endometrial cancer | |||||||||||||
Medical condition: Recurrent endometrial cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: IT (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-003604-21 | Sponsor Protocol Number: KT-IBA | Start Date*: 2011-10-24 | |||||||||||
Sponsor Name:Universitätsklinik für Innere Medizin IV, Medizinische Universität Innsbruck | |||||||||||||
Full Title: The role of immunosuppressives in immunosenescence and immunotolerance in renal transplantation | |||||||||||||
Medical condition: The impact of immunosuppressives on age-related changes of the immune system will be analyzed in patients after renal transplantation. Only patients at least one year after renal tranplantation and... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: AT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-004539-22 | Sponsor Protocol Number: 11-2012 | Start Date*: 2013-03-18 | |||||||||||
Sponsor Name:I.T.M.O. - ITALIAN TRIALS IN MEDICAL ONCOLOGY | |||||||||||||
Full Title: An open label, single arm, phase II study to evaluate the activity and toxicity of Panitumumab in pre-treated patients with advanced well differentiated neuroendocrine tumor (G1 and G2) | |||||||||||||
Medical condition: Well differentiated neuroendocrine tumor (G1 and G2) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2021-000823-11 | Sponsor Protocol Number: TIMO | Start Date*: 2023-03-09 | ||||||||||||||||
Sponsor Name:Sahlgrenska University Hospital Gothenburg | ||||||||||||||||||
Full Title: Ticagrelor monotherapy after coronary stenting in patients with acute myocardial infarction. A prospective single-centre, single-arm phase II study | ||||||||||||||||||
Medical condition: Antiplatelet therapy in patients who undergo coronary artery stenting due to coronary artery disease (CAD) or acute coronary syndrome (ACS). The present study will examine whether ticagrelor, as mo... | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: SE (Trial now transitioned) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-001207-68 | Sponsor Protocol Number: KKSH140 | Start Date*: 2018-11-20 | ||||||||||||||||
Sponsor Name:Martin-Luther-Universität Halle-Wittenberg | ||||||||||||||||||
Full Title: A multicenter single-arm pilot study of ramucirumab in combination with dacarbazine in patients with progressive well-differentiated metastatic pancreatic neuroendocrine tumors | ||||||||||||||||||
Medical condition: Progressive well-differentiated metastatic pancreatic neuroendocrine tumors | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: DE (Trial now transitioned) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2010-021755-34 | Sponsor Protocol Number: 2010-021755-34 | Start Date*: 2010-07-22 | |||||||||||||||||||||
Sponsor Name:ISTITUTO NAZIONALE PER LA CURA TUMORI | |||||||||||||||||||||||
Full Title: Phase II study on imatinib in combination with RAD001 in advanced chordoma | |||||||||||||||||||||||
Medical condition: PDGFRB and mTOR (or S6 or 4BP1) positive advanced chordoma | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: IT (Completed) | |||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2018-002190-21 | Sponsor Protocol Number: MAR-BAS-18-005 | Start Date*: 2020-07-08 | |||||||||||||||||||||
Sponsor Name:Fondazione per la Medicina Personalizzata | |||||||||||||||||||||||
Full Title: The ROME trial from histology to target: the road to personalize target therapy and immunotherapy | |||||||||||||||||||||||
Medical condition: Patients with progressive disease (recurrent and/or metastatic) of breast cancer, metastatic gastro-intestinal tumors, non small cell lung cancer (NSCLC) or others. Patients should have completed a... | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: IT (Completed) | |||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2004-003018-41 | Sponsor Protocol Number: CRAD001C2235 | Start Date*: 2005-08-18 |
Sponsor Name:Novartis Pharma Services AG | ||
Full Title: Open label, non-randomized, phase 2 Study investigating the effect of RAD001 monotherapy in patients with advanced NSCLC previously treated with either chemotherapy only or with chemotherapy and EG... | ||
Medical condition: Lung cancer is one of the most common malignancies in developed countries and accounts for millions of deaths worldwide. In 2000, the annual incidence of non-small cell lung cancer (NSCLC), which c... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Completed) IT (Completed) | ||
Trial results: View results |
EudraCT Number: 2015-005616-14 | Sponsor Protocol Number: M13-596 | Start Date*: 2016-05-31 |
Sponsor Name:AbbVie Deutschland GmbH & Co. KG | ||
Full Title: A Single-Arm, Open-Label, Multicenter Study to Evaluate the Safety and Efficacy of ABT-493/ABT-530 in Adult Post-Liver or Post-Renal Transplant Recipients with Chronic Hepatitis C Virus Genotype 1 ... | ||
Medical condition: Hepatitis C Virus | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) ES (Completed) | ||
Trial results: View results |
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