- Trials with a EudraCT protocol (85)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (48)
85 result(s) found for: AKT.
Displaying page 1 of 5.
EudraCT Number: 2011-002576-16 | Sponsor Protocol Number: GINECO-EN102b | Start Date*: 2013-06-11 |
Sponsor Name:ARCAGY | ||
Full Title: Phase 2 multicenter study to assess the safety and efficacy of BKM120 as monotherapy in the treatment of initial or recurrent metastatic endometrial cancer after first line therapy in patients who ... | ||
Medical condition: initial or recurrent metastatic endometrial cancer after first line therapy in patients who cannot undergo local surgery and/or radiotherapy. | ||
Disease: | ||
Population Age: Adults | Gender: Female | |
Trial protocol: FR (Completed) | ||
Trial results: View results |
EudraCT Number: 2006-001031-22 | Sponsor Protocol Number: CCR2749 | Start Date*: 2007-12-18 |
Sponsor Name:Institute of Cancer Research | ||
Full Title: The Potentiation of Efficacy of Radiotherapy in Non-Small-Cell Lung Cancer (NSCLC) by Inhibition of Akt Activation | ||
Medical condition: Non-small-cell lung cancer | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Prematurely Ended) | ||
Trial results: (No results available) |
EudraCT Number: 2012-005019-14 | Sponsor Protocol Number: 12076 | Start Date*: 2013-05-03 | |||||||||||
Sponsor Name:University of Nottingham | |||||||||||||
Full Title: The short term effects of an AKT inhibitor (AZD5363) on biomarkers of the AKT pathway and anti-tumour activity in a breast cancer paired biopsy study (STAKT Trial) | |||||||||||||
Medical condition: primary breast cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-000182-10 | Sponsor Protocol Number: CBI-GBM-01 | Start Date*: 2006-05-04 |
Sponsor Name:Rigshospitalet, Finsen Center | ||
Full Title: A phase II trial with cetuximab, bevacizumab and irinotecan for patients with malignant glioblastomas and progression after radiation therapy and temozolamid | ||
Medical condition: Recurrent or progressive primary GBM in patients with performance status (PS) 0-2. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DK (Completed) | ||
Trial results: View results |
EudraCT Number: 2017-003040-20 | Sponsor Protocol Number: MX39795 | Start Date*: 2018-06-20 | |||||||||||
Sponsor Name:F. Hoffmann-La Roche Ltd | |||||||||||||
Full Title: A phase II, randomized, active-controlled, multi-center study comparing the efficacy and safety of targeted therapy or cancer immunotherapy guided by genomic profiling versus platinum-based chemoth... | |||||||||||||
Medical condition: Cancer of Unknown Primary Site | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) AT (Completed) EE (Completed) IE (Completed) DE (Completed) CZ (Completed) FI (Completed) LV (Completed) HU (Completed) PL (Completed) FR (Completed) ES (Ongoing) BG (Completed) PT (Completed) HR (Completed) NO (Completed) NL (Completed) DK (Completed) CY (Prematurely Ended) IT (Completed) RO (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2004-001712-31 | Sponsor Protocol Number: | Start Date*: 2005-01-24 |
Sponsor Name:Lothian Health - University Hospitals Division | ||
Full Title: A study to evaluate the biological effects of RAD001 on invasive breast cancer | ||
Medical condition: Breast Cancer | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2008-003679-40 | Sponsor Protocol Number: BEV-CCI-779-GBM-02 | Start Date*: 2008-09-03 | |||||||||||
Sponsor Name:Rigshospitalet | |||||||||||||
Full Title: A phase II study of temsirolimus and bevacizumab in recurrent glioblastoma multiforme | |||||||||||||
Medical condition: Glioblastoma multiforme and progression after prior VEGF-directed therapy | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-006119-22 | Sponsor Protocol Number: FARM6HJ7CA | Start Date*: 2008-03-25 |
Sponsor Name:UNIVERSITA' DEGLI STUDI DI NAPOLI FEDERICO II | ||
Full Title: Phase II monitored clinical trial for evaluation of treatment of patients with Thymic Epithelial Tumours (TET) or Histiocitosi X (LCH) with Imatinib Mesylate. | ||
Medical condition: Patients affected by TET or LCH | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: IT (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2014-003029-16 | Sponsor Protocol Number: GO29505 | Start Date*: 2014-12-01 | |||||||||||
Sponsor Name:Genentech, Inc. | |||||||||||||
Full Title: A phase II randomized, double-blind study of ipatasertib (GDC-0068), an inhibitor to Akt in combination with paclitaxel as neoadjuvant treatment for patients with early stage triple negative breast... | |||||||||||||
Medical condition: Early stage triple negative breast cancer. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: ES (Completed) PT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-000728-41 | Sponsor Protocol Number: 06/02-29 jan'07 | Start Date*: 2008-09-12 | ||||||||||||||||
Sponsor Name:Maastro clinic | ||||||||||||||||||
Full Title: A phase I/II trial testing nelfinavir, an inhibitor of Akt signaling, in combination with preoperative chemoradiotherapy in patients with locally advanced rectal cancer | ||||||||||||||||||
Medical condition: A phase I/II trial testing nelfinavir, an inhibitor of Akt signaling, in combination with preoperative chemoradiotherapy with locally advanced rectal cancer | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: NL (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2011-002167-23 | Sponsor Protocol Number: IPC_2011-001 | Start Date*: 2013-06-12 | |||||||||||
Sponsor Name:Institut Paoli-Calmettes | |||||||||||||
Full Title: A phase Ib/II open-label study evaluating safety and efficacy of oral BKM120 in combination with lapatinib in HER2+/PI3K-activated, trastuzumab-resistant locally advanced, recurrent and metastatic ... | |||||||||||||
Medical condition: locally advanced, recurrent and metastatic breast cancer. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-004558-24 | Sponsor Protocol Number: CC-115-ST-001 | Start Date*: 2012-06-29 | |||||||||||
Sponsor Name:Celgene Corporation | |||||||||||||
Full Title: A PHASE 1A/1B, MULTICENTER, OPEN LABEL, DOSE-FINDING STUDY TO ASSESS THE SAFETY, TOLERABILITY, PHARMACOKINETICS AND PRELIMINARY EFFICACY OF THE DUAL DNA-PK AND TOR KINASE INHIBITOR, CC-115, ADMINIS... | |||||||||||||
Medical condition: Subjects with advanced solid tumors, non-hodgkin lymphoma (NHL) and multiple myeloma (MM). | |||||||||||||
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Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) FR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-005219-16 | Sponsor Protocol Number: GE-135-003 | Start Date*: 2010-12-06 |
Sponsor Name:GE Healthcare Ltd | ||
Full Title: A Phase 2, Open-label, Proof-of-concept Study to Assess the Ability to Detect Tumours and Angiogenesis via the Expression of avb3 Integrin Receptors by [18F]AH111585 PET Imaging | ||
Medical condition: Adult subjects with Primary or metastatic tumour lesion of one of the following types: high-grade glioma, including GBM, anaplastic astrocytoma, and anaplastic oligodendroglioma; lung cancer, inclu... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2008-004431-38 | Sponsor Protocol Number: P15099 | Start Date*: 2009-02-20 | |||||||||||
Sponsor Name:Imperial College | |||||||||||||
Full Title: ACE inhibition and mechanisms of skeletal muscle weakness in COPD | |||||||||||||
Medical condition: Chronic obstructive pulmonary disease patients who have skeletal muscle weakness. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-002497-37 | Sponsor Protocol Number: IOV-SCLC-1-2014-TIMES | Start Date*: 2014-12-22 | |||||||||||
Sponsor Name:Istituto Oncologico del Veneto IRCCS – UOC Oncologia Medica 2 | |||||||||||||
Full Title: TIvantinib as Maintenance treatment in Extended Small-cell lung cancer (TIMES) Phase II clinical trial, single arm, two stage | |||||||||||||
Medical condition: Small Cell Lung Cancer (SCLC) after first-line platinum plus etoposide therapy | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-002080-10 | Sponsor Protocol Number: GO28341 | Start Date*: 2013-10-29 | ||||||||||||||||
Sponsor Name:Genentech, Inc. | ||||||||||||||||||
Full Title: A RANDOMIZED, PHASE II, PLACEBO-CONTROLLED STUDY OF GDC-0068, AN INHIBITOR TO AKT, IN COMBINATION WITH FLUOROPYRIMIDINE PLUS OXALIPLATIN IN PATIENTS WITH LOCALLY ADVANCED OR METASTATIC GASTRIC OR G... | ||||||||||||||||||
Medical condition: Inoperable locally advanced or metastatic or recurrent gastric or gastroesophageal adenocarcinoma. | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) DE (Completed) IT (Completed) ES (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2014-000469-35 | Sponsor Protocol Number: GO29227 | Start Date*: 2014-08-12 | ||||||||||||||||
Sponsor Name:Genentech, Inc. | ||||||||||||||||||
Full Title: A RANDOMIZED, PHASE II, MULTICENTER, PLACEBO-CONTROLLED STUDY OF IPATASERTIB (GDC-0068), AN INHIBITOR OF AKT, IN COMBINATION WITH PACLITAXEL AS FRONT-LINE TREATMENT FOR PATIENTS WITH METASTATIC TRI... | ||||||||||||||||||
Medical condition: Inoperable locally advanced or metastatic triple negative breast cancer | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Female | |||||||||||||||||
Trial protocol: IT (Completed) BE (Completed) ES (Completed) FR (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2007-001174-81 | Sponsor Protocol Number: D07-1 | Start Date*: 2007-06-25 | |||||||||||
Sponsor Name:GERCOR | |||||||||||||
Full Title: RANDOMIZED MULTICENTER PHASE III STUDY IN PATIENTS WITH LOCALLY ADVANCED ADENOCARCINOMA OF THE PANCREAS: GEMCITABINE WITH OR WITHOUT CHEMORADIOTHERAPY AND WITH OR WITHOUT ERLOTINIB | |||||||||||||
Medical condition: Patients with de novo locally advanced, histologically proven adenocarcinoma of the pancreas without distant metastases (stage III according to the UICC classification) and not considered for curat... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) BE (Completed) SE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2018-004520-10 | Sponsor Protocol Number: ACNS1021 | Start Date*: 2019-06-25 |
Sponsor Name:National Cancer Institute (NCI) | ||
Full Title: 2018-004520-10 | ||
Medical condition: Recurrent, Refractory or Progressive High Grade Glioma and Ependymoma Tumors | ||
Disease: | ||
Population Age: Infants and toddlers, Children, Adolescents, Under 18, Adults | Gender: Male, Female | |
Trial protocol: Outside EU/EEA | ||
Trial results: View results |
EudraCT Number: 2006-001238-41 | Sponsor Protocol Number: 2006-001238-41 | Start Date*: 2007-01-04 | |||||||||||
Sponsor Name:AZIENDA OSPEDALIERA POLICLINICO DI MODENA | |||||||||||||
Full Title: Phase II trial of Erlotinib in combination with increasing dose of gemcitabine given as fixed dose rate infusion in advanced pancreatic cancer. | |||||||||||||
Medical condition: Patients with unresectable advanced or metastatic pancreatic cancer | |||||||||||||
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Population Age: Children, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
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