- Trials with a EudraCT protocol (314)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (1)
314 result(s) found for: Everolimus.
Displaying page 16 of 16.
EudraCT Number: 2015-004851-28 | Sponsor Protocol Number: EVG001BC | Start Date*: 2016-12-07 |
Sponsor Name:Evgen Pharma PLC | ||
Full Title: A Multicentre Phase 2 Study of SFX-01 Treatment and Evaluation in Patients with Estrogen Receptor (ER) Positive and Human Epidermal Growth Factor Receptor 2 (HER2) Negative Metastatic Breast Cancer... | ||
Medical condition: Estrogen Receptor (ER) Positive and Human Epidermal Growth Factor Receptor 2 (HER2) Negative Metastatic Breast Cancer Progressing on either an Aromatase Inhibitor (AI) or Tamoxifen or Fulvestrant | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) ES (Completed) FR (Completed) | ||
Trial results: View results |
EudraCT Number: 2014-004010-28 | Sponsor Protocol Number: I3Y-MC-JPBO | Start Date*: 2015-03-10 | |||||||||||
Sponsor Name:Eli Lilly and Company | |||||||||||||
Full Title: A Phase 2 Study of Abemaciclib in Patients with Brain Metastases Secondary to Hormone Receptor Positive Breast Cancer, Non-small Cell Lung Cancer, or Melanoma | |||||||||||||
Medical condition: Brain tumors, Breast Cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: AT (Completed) BE (Completed) FR (Completed) ES (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-000454-32 | Sponsor Protocol Number: C/23/2011 | Start Date*: 2012-01-17 | |||||||||||
Sponsor Name:Imperial College London | |||||||||||||
Full Title: A single arm phase IIa study (with combination safety run-in) to assess the safety and efficacy of AZD4547 in combination with either anastrozole or letrozole in ER positive breast cancer patients ... | |||||||||||||
Medical condition: ER Positive Progressing Breast Cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2016-001468-12 | Sponsor Protocol Number: PEN-221-001 | Start Date*: 2017-01-16 |
Sponsor Name:Tarveda Therapeutics, Inc. | ||
Full Title: A Phase 1/2a, open-label multicenter study to assess the safety, tolerability, pharmacokinetics, and preliminary antitumor activity of PEN-221 in patients with somatostatin receptor 2 expressing ad... | ||
Medical condition: Somatostatin receptor 2 (SSTR2) expressing advanced cancers, including gastroenteropancreatic (GEP) cancer or lung cancer or thymus cancer or other NETs (Neuroendocrine tumour) or small cell lung c... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (GB - no longer in EU/EEA) | ||
Trial results: (No results available) |
EudraCT Number: 2018-003896-37 | Sponsor Protocol Number: ODO-TE-B201 | Start Date*: 2019-06-18 | ||||||||||||||||||||||||||||||||||||
Sponsor Name:Odonate Therapeutics, Inc. | ||||||||||||||||||||||||||||||||||||||
Full Title: A Multinational, Multicenter, Phase 2 Study of Tesetaxel plus a Reduced Dose of Capecitabine in Patients with HER2 Negative, Hormone Receptor Positive, Locally Advanced or Metastatic Breast Cancer ... | ||||||||||||||||||||||||||||||||||||||
Medical condition: breast cancer | ||||||||||||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||||||||||||
Trial protocol: ES (Prematurely Ended) | ||||||||||||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-005806-38 | Sponsor Protocol Number: NO21884 | Start Date*: 2009-10-23 | ||||||||||||||||||||||||||
Sponsor Name:F.Hoffmann-La Roche Ltd. | ||||||||||||||||||||||||||||
Full Title: A multiple ascending dose study to evaluate the safety, tolerability and effect on tumor response of the mTOR inhibitor (RAD001) in combination with the IGF-1R antagonist (R1507) in patients with a... | ||||||||||||||||||||||||||||
Medical condition: PIb: solid malignancy that is metastatic or unresectable PII: C 1: Advanced metastatic renal cell carcinoma C 2: Advanced low- to intermediate grade metastatic or unresectable locoregional pancre... | ||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: FR (Completed) | ||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2020-003395-41 | Sponsor Protocol Number: EVIDENT | Start Date*: 2021-01-15 | |||||||||||
Sponsor Name:Oslo University Hospital | |||||||||||||
Full Title: An open-label single arm interventional phase 2 study to investigate outcome of individualized treatment based on pharmacogenomic profiling and ex vivo drug sensitivity testing of patient-derived o... | |||||||||||||
Medical condition: Metastatic Colorectal Cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NO (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2015-002824-18 | Sponsor Protocol Number: 8-311-3-062 | Start Date*: Information not available in EudraCT | ||||||||||||||||
Sponsor Name:AZIENDA OSPEDALIERO-UNIVERSITARIA PISANA | ||||||||||||||||||
Full Title: A PHASE II, RANDOMIZED, CROSS-OVER, DOUBLE-BLIND, PLACEBO-CONTROLLED, SINGLE CENTER STUDY OF THE EFFECTS OF DAPAGLIFLOZIN VS PLACEBO ON ENDOGENOUS GLUCOSE PRODUCTION IN RENAL TRANSPLANT SUBJECTS WI... | ||||||||||||||||||
Medical condition: RENAL TRANSPLANT SUBJECTS WITH OR WITHOUT TYPE 2 DIABETES AND TYPE 2 DIABETIC SUBJECTS WITH NORMAL RENAL FUNCTION | ||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | |||||||||||||||||
Trial protocol: IT (Completed) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2019-002186-36 | Sponsor Protocol Number: DSC-BROMS-1 | Start Date*: 2021-05-26 | |||||||||||
Sponsor Name:Uppsala University Hospital | |||||||||||||
Full Title: A multicenter, open-label, randomized, phase I/II clinical trial comparing safety and durable overall response rate (DOR) at 56 days in patients with steroid resistant severe acute GvHD after allog... | |||||||||||||
Medical condition: Steroid refractory acute GVHD | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Trial now transitioned) NO (Trial now transitioned) DK (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2013-001363-23 | Sponsor Protocol Number: MetAction | Start Date*: 2014-10-29 | |||||||||||||||||||||||||||||||||||||||||
Sponsor Name:Oslo University Hospital | |||||||||||||||||||||||||||||||||||||||||||
Full Title: N-of-1 trial: Actionable Target Identification in Metastatic Cancer for Palliative Systemic Therapy | |||||||||||||||||||||||||||||||||||||||||||
Medical condition: Patients with actionable target identified in metastatic cancer for palliative systemic treatment. | |||||||||||||||||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||||||||||||||||||||||
Trial protocol: NO (Completed) | |||||||||||||||||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2020-005107-40 | Sponsor Protocol Number: SNDX-6352-0504 | Start Date*: 2021-08-24 | |||||||||||
Sponsor Name:Syndax Pharmaceuticals, Inc. | |||||||||||||
Full Title: AGAVE-201, A Phase 2, Open-label, Randomized, Multicenter Study to Evaluate the Efficacy, Safety and Tolerability of Axatilimab at 3 Different Doses in Patients with Recurrent or Refractory Active ... | |||||||||||||
Medical condition: Recurrent/Refractory Active Chronic Graft Versus Host Disease | |||||||||||||
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Population Age: Children, Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Trial now transitioned) BE (Trial now transitioned) IT (Trial now transitioned) ES (Ongoing) PT (Completed) GR (Trial now transitioned) FR (Trial now transitioned) | |||||||||||||
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: 2010-024425-20 | Sponsor Protocol Number: Esperanz-002 | Start Date*: 2011-03-14 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Sponsor Name:Leiden University Medical Centre | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Full Title: Phase III Randomized Double-blind Cross-over trial of Supersaturated Calcium-phosphate rinse (Caphosol®) versus NaCl 0.9% in the relief of Oral Mucositis in renal cell carcinoma, hepatocellular car... | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Medical condition: oral mucositis in renal cell carcinoma, hepatocellular carcinoma, and gastrointestinal stromal tumor | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Trial protocol: NL (Ongoing) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2015-001467-39 | Sponsor Protocol Number: GETNE1509 | Start Date*: 2015-07-24 | ||||||||||||||||
Sponsor Name:GETNE (Grupo Español de Tumores Neuroendocrinos) | ||||||||||||||||||
Full Title: A phase II study to evaluate the safety and efficacy of lenvatinib in patients with advanced grade 1/2 neuroendocrine neoplasmas of pancreatic and extrapancreatic origin. | ||||||||||||||||||
Medical condition: Patients with advanced/metastatic, histologically confirmed, grade 1/2 (G1/G2) of 2010 WHO classification neuroendocrine tumors of the pancreas after progression to a previous targeted agent (cohor... | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: ES (Ongoing) AT (Completed) IT (Completed) | ||||||||||||||||||
Trial results: View results |
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