- Trials with a EudraCT protocol (294)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
294 result(s) found for: In situ hybridization.
Displaying page 3 of 15.
EudraCT Number: 2011-005002-30 | Sponsor Protocol Number: ICORG09-13 | Start Date*: 2012-01-05 | |||||||||||
Sponsor Name:ICORG-the All Ireland co-operative Oncology Research group | |||||||||||||
Full Title: Phase II Lap/Epi: Phase II evaluation of the combination of epirubicin and lapatinib in Her-2 positive, Topoisomerase II alpha positive, metastatic breast cancer. | |||||||||||||
Medical condition: Metastatic breast cancer in patients who are HER-2-positive and Topoisomerase II alpha positive. | |||||||||||||
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Population Age: | Gender: Female | ||||||||||||
Trial protocol: IE (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-002207-15 | Sponsor Protocol Number: Cardiorete | Start Date*: 2011-12-27 |
Sponsor Name:FONDAZIONE DEL PIEMONTE PER L'ONCOLOGIA IRCC DI CANDIOLO | ||
Full Title: A prospective study with beta-blockers and ACE-inhibitors in patients operable breast cancer experiencing mild cardiac toxicity during treatment with anthracycline and/or trastuzumab | ||
Medical condition: patients experiencing mild cardiotoxicity during treatment with anthracycline and/or trastuzumab for operable breast cancer | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Female | |
Trial protocol: IT (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2018-004121-80 | Sponsor Protocol Number: | Start Date*: 2019-02-05 | |||||||||||
Sponsor Name:The Christie Hospital NHS Foundation Trust | |||||||||||||
Full Title: A proof of concept, window trial of the IMmunological effects of AveLumab and Aspirin in Triple-Negative Breast Cancer. | |||||||||||||
Medical condition: Breast Cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2013-002684-25 | Sponsor Protocol Number: SICOG13/01 | Start Date*: 2014-03-19 | |||||||||||
Sponsor Name:S.I.C.O.G. ONLUS | |||||||||||||
Full Title: Phase II study of liposomal doxorubicin in combination with trastuzumab plus cyclophosphamide followed by docetaxel plus trastuzumab as primary systemic therapy for patients with locally advanced ... | |||||||||||||
Medical condition: Local advanced breast cancer resectable, neoadjuvant setting | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-000167-25 | Sponsor Protocol Number: UC-0110/1201 | Start Date*: 2012-05-29 | |||||||||||
Sponsor Name:UNICANCER | |||||||||||||
Full Title: A multicentric randomized phase II study evaluating dual targeting of the EGFR using the combination of cetuximab and afatinib versus cetuximab alone in patients with chemotherapy refractory wtKRAS... | |||||||||||||
Medical condition: Refractory wtKRAS metastatic colorectal cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2018-004247-23 | Sponsor Protocol Number: LUMC201811 | Start Date*: 2019-03-22 |
Sponsor Name:Leiden University Medical Center | ||
Full Title: [89Zr]trastuzumab PET/CT imaging of HER2 positive breast cancer for predicting pathologic complete response after neoadjuvant chemotherapy; A multicentre study | ||
Medical condition: HER2+ breast cancer | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Female | |
Trial protocol: NL (Prematurely Ended) | ||
Trial results: (No results available) |
EudraCT Number: 2015-002801-12 | Sponsor Protocol Number: ONT-380-206 | Start Date*: 2017-08-07 | |||||||||||
Sponsor Name:Seagen Inc. | |||||||||||||
Full Title: Phase 2 Randomized, Double-Blinded, Controlled Study of Tucatinib vs. Placebo in Combination with Capecitabine and Trastuzumab in Patients with Pretreated Unresectable Locally Advanced or Metastati... | |||||||||||||
Medical condition: Pretreated Unresectable Locally Advanced or Metastatic HER2+ Breast Carcinoma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) AT (Completed) CZ (Completed) BE (Completed) DK (Completed) FR (Completed) PT (Completed) GB (GB - no longer in EU/EEA) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2016-002893-11 | Sponsor Protocol Number: PASIPHAE | Start Date*: 2017-08-14 |
Sponsor Name:Karolinska University Hospital | ||
Full Title: A phase 2, international, multicenter, open-labeled, randomized trial of PAlbociclib and fulvestrant vs. Standard oral capecitabine In Patients with Hormone receptor positive/HER2 negative Advanced... | ||
Medical condition: Hormone receptor positive/HER2 negative advanced breast cancer with endocrine resistance | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Female | |
Trial protocol: SE (Prematurely Ended) GB (GB - no longer in EU/EEA) | ||
Trial results: (No results available) |
EudraCT Number: 2006-001197-24 | Sponsor Protocol Number: D791AC00011 | Start Date*: 2006-09-18 |
Sponsor Name:AstraZeneca AB | ||
Full Title: A Phase II, Double-blind, Randomised, Parallel Group, Multi-centre Study Comparing gefitinib 250 mg (IRESSA™) with erlotinib 150 mg (Tarceva®) in Previously Treated Patients with Locally Advanced o... | ||
Medical condition: Non-small Cell Lung Cancer | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: BE (Completed) AT (Completed) DE (Completed) GB (GB - no longer in EU/EEA) | ||
Trial results: (No results available) |
EudraCT Number: 2005-000104-13 | Sponsor Protocol Number: B-02 | Start Date*: 2005-08-05 |
Sponsor Name:Translational Oncology Research International | ||
Full Title: A multicenter, placebo-controlled, double-blind randomised phase II trial of neoadjuvant treatment with single-agent bevacizumab or placebo, followed by six cycles of docetaxel, doxorubucin, and cy... | ||
Medical condition: Stage II or Stage III breast cancer | ||
Disease: | ||
Population Age: Adults | Gender: Female | |
Trial protocol: IE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2017-000129-12 | Sponsor Protocol Number: PCYC-1143-CA | Start Date*: 2017-10-10 | |||||||||||
Sponsor Name:Pharmacyclics LLC | |||||||||||||
Full Title: Phase 3 Study of Ibrutinib in Combination with Venetoclax in Subjects with Mantle Cell Lymphoma | |||||||||||||
Medical condition: Mantle Cell Lymphoma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) CZ (Completed) DE (Completed) BE (Completed) HU (Completed) ES (Ongoing) NL (Completed) GR (Completed) IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2005-004350-28 | Sponsor Protocol Number: VEG20007 | Start Date*: 2006-08-22 |
Sponsor Name:GlaxoSmithKline Research & Development Limited | ||
Full Title: A Phase II, Open-Label, Randomized, Multicenter Trial of GW786034 (Pazopanib) in Combination with Lapatinib (GW572016) Compared to Lapatinib Alone as First Line Therapy in Subjects with Advanced or... | ||
Medical condition: Advanced or metastatic breast cancer with ErbB2 FISH postive tumours | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Female | |
Trial protocol: GB (Completed) HU (Completed) | ||
Trial results: View results |
EudraCT Number: 2012-000134-19 | Sponsor Protocol Number: AEZS-108-049 | Start Date*: 2012-09-07 | |||||||||||
Sponsor Name:Aeterna Zentaris GmbH | |||||||||||||
Full Title: A randomised, phase 2 trial of AEZS-108 in chemotherapy refractory triple negative (ER/PR/HER2-negative) LHRH-R positive metastatic breast cancer | |||||||||||||
Medical condition: Histologically confirmed malignancy of breast tissue; estrogen- and progesterone receptor negative, non overexpressing HER2-receptors, LHRH receptor positive tumor status; receptor status determine... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-003176-21 | Sponsor Protocol Number: TRIO 017 | Start Date*: 2008-12-31 | |||||||||||
Sponsor Name:Cancer International Research Group | |||||||||||||
Full Title: A phase II, open label multicenter trial of panobinostat (LBH589) monotherapy in women with HER2 negative locally recurrent or metastatic breast cancer | |||||||||||||
Medical condition: Women with HER-2 negative locally recurrent or metastatic breast cancer; | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: FR (Completed) BE (Completed) IE (Completed) GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2016-001407-23 | Sponsor Protocol Number: GEICAM/2015-06 | Start Date*: 2017-01-05 | |||||||||||
Sponsor Name:GEICAM (Fundación Grupo Español de Investigación en Cáncer de Mama) | |||||||||||||
Full Title: A Phase II Clinical Trial to analyse Olaparib Response in patients with BRCA1 and/or 2 Promoter Methylation Diagnosed of Advanced Breast Cancer (COMETA-Breast study). | |||||||||||||
Medical condition: Patients with advanced triple negative breast cancer (TNBC) with BRCA1 and/or BRCA2 promoter methylation assessed in DNA from metastatic lesions and absence of BRCA1 and 2 germline mutations. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: ES (Ongoing) | |||||||||||||
Trial results: View results |
EudraCT Number: 2015-002323-25 | Sponsor Protocol Number: FBCG-01-2015 | Start Date*: 2015-06-25 |
Sponsor Name:Finnish Breast Cancer Group | ||
Full Title: A randomized phase III study comparing trastuzumab, pertuzumab plus docetaxel (TPD) followed by 3 cycles of chemotherapy to the current standard regimen as the treatments of early HER2-positive bre... | ||
Medical condition: Early HER-2 -positive breast cancer | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Female | |
Trial protocol: FI (Trial now transitioned) SE (Trial now transitioned) | ||
Trial results: (No results available) |
EudraCT Number: 2017-004176-62 | Sponsor Protocol Number: CLEE011AIT01 | Start Date*: 2018-01-10 | |||||||||||
Sponsor Name:NOVARTIS FARMA S.P.A. | |||||||||||||
Full Title: A phase IIIb, open-label, local, multicenter study of the molecular features of postmenopausal women with hormone receptor-positive (HR+) HER2-negative advanced breast cancer on first-line treatmen... | |||||||||||||
Medical condition: Hormone receptor-positive (HR+) HER2-negative advanced breast cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: IT (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2020-005792-12 | Sponsor Protocol Number: GOIRC-06-2020 | Start Date*: 2022-04-05 | |||||||||||
Sponsor Name:GRUPPO ONCOLOGICO ITALIANO DI RICERCA CLINICA (GOIRC) | |||||||||||||
Full Title: Pilot ‘Window of Opportunity’ Neoadjuvant Study of Abemaciclib in Low-Estrogen Receptor (ER) positive/Human Epidermal Growth Factor Receptor 2 (HER2)-negative Early Breast Cancer (BC) | |||||||||||||
Medical condition: Low-Estrogen Receptor (ER) positive/Human Epidermal Growth Factor Receptor 2 (HER2)-negative Early Breast Cancer (BC) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-000394-23 | Sponsor Protocol Number: SOLTI-1007 | Start Date*: 2012-08-06 |
Sponsor Name:SOLTI | ||
Full Title: A Phase II, open-label, single-arm, exploratory pharmacogenomic study of single agent eribulin (HALAVEN®) as neoadjuvant treatment for operable Stage I-II HER2 non-overexpressing breast cancer | ||
Medical condition: Patients at Stage I-II HER2-negative breast cancer | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: ES (Completed) DE (Completed) PT (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2008-008276-14 | Sponsor Protocol Number: BO22495 | Start Date*: 2009-04-27 | ||||||||||||||||
Sponsor Name:F. Hoffmann-la Roche Ltd | ||||||||||||||||||
Full Title: A Phase Ib/II, open-label study of the safety, tolerability, and efficacy of trastuzumab-MCC-DM1 in combination with pertuzumab administered intravenously to patients with HER2-positive locally adv... | ||||||||||||||||||
Medical condition: Treatment in patients with HER2-overexpressing locally advanced or metastatic breast cancer | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: FR (Completed) DE (Completed) BE (Completed) | ||||||||||||||||||
Trial results: View results |
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