- Trials with a EudraCT protocol (175)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
175 result(s) found for: Core Needle Biopsy.
Displaying page 1 of 9.
EudraCT Number: 2019-003582-18 | Sponsor Protocol Number: 20190009 | Start Date*: 2020-05-18 |
Sponsor Name:Amgen, Inc. | ||
Full Title: A Phase 3 Multicenter, Randomized, Open Label, Active-controlled, Study of AMG 510 Versus Docetaxel for the Treatment of Previously Treated Locally Advanced and Unresectable or Metastatic NSCLC S... | ||
Medical condition: Previously treated locally advanced and unresectable or metastatic nonsmall cell lung cancer (NSCLC) with KRAS p.G12C mutation | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (GB - no longer in EU/EEA) SE (Ongoing) FR (Trial now transitioned) DK (Completed) PL (Ongoing) FI (Completed) BE (Completed) PT (Completed) DE (Ongoing) NL (Trial now transitioned) ES (Ongoing) HU (Ongoing) GR (Trial now transitioned) IT (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2005-001417-18 | Sponsor Protocol Number: DTS-301CLI001 | Start Date*: 2005-09-27 |
Sponsor Name:DIATOS S.A. | ||
Full Title: A Phase II Clinical Trial to Evaluate Intratumoral Injection of a Depot Formulation of Paclitaxel (DTS-301) as Neoadjuvant Therapy of Patients with Breast Cancer | ||
Medical condition: Invasive primary breast cancer | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Female | |
Trial protocol: AT (Prematurely Ended) HU (Prematurely Ended) | ||
Trial results: (No results available) |
EudraCT Number: 2005-000403-33 | Sponsor Protocol Number: GEICAM/2004-04 | Start Date*: 2005-06-01 |
Sponsor Name:GRUPO ESPAÑOL DE INVESTIGACIÓN EN CÁNCER DE MAMA (GEICAM) | ||
Full Title: Randomized clinical trial to evaluate the predictive accuracy of a gene expression profile-based test to select patients for preoperative taxane/anthracycline chemotherapy for stage I-III breast ca... | ||
Medical condition: Patients with histologically confirmed stage I-III invasive carcinoma of the breast for whom adjuvant chemotherapy is indicated. | ||
Disease: | ||
Population Age: Adults | Gender: Female | |
Trial protocol: ES (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2005-005715-22 | Sponsor Protocol Number: D6990C00001 | Start Date*: 2006-02-21 |
Sponsor Name:AstraZeneca AB | ||
Full Title: A randomised Phase II Study comparing anastrozole and fulvestrant to an-astrozole for adjuvant treatment of postmenopausal patients with early breast cancer and disseminated tumour cells in bone ma... | ||
Medical condition: postmenopausal women with hormone receptor positive early breast cancer | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Female | |
Trial protocol: AT (Prematurely Ended) NO (Completed) DE (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2005-000661-19 | Sponsor Protocol Number: CFEM345EGB07 | Start Date*: 2005-11-04 |
Sponsor Name:Novartis Pharmaceuticals UK Ltd | ||
Full Title: Neoadjuvant hormone therapy for postmenopausal women with ER and/or PgR positive primary breast cancer: A multi-center study to determine the optimum length of treatment with Femara (letrozole 2.5m... | ||
Medical condition: Postmenopausal women with ER and/or PgR positive primary breast cancer | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Female | |
Trial protocol: GB (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2012-003126-25 | Sponsor Protocol Number: MS201923-0001 | Start Date*: 2012-09-27 | |||||||||||
Sponsor Name:Merck KGaA | |||||||||||||
Full Title: An Open-Label, First-in-Human Study of the Safety, Tolerability, and Pharmacokinetics of VX-970/M6620 in Combination With Cytotoxic Chemotherapy in Participants With Advanced Solid Tumors | |||||||||||||
Medical condition: cancer (malignant solid tumors) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2019-002991-15 | Sponsor Protocol Number: SOLTI-1804 | Start Date*: 2019-11-04 |
Sponsor Name:SOLTI | ||
Full Title: HER2-PREDICT: Estudio Traslacional De Muestras De Tumor Procedentes De Los Ensayos Ds8201-A-U301 y Ds8201-A-U302 | ||
Medical condition: Her2‑positive, unresectable and/or metastatic breast cancer. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Female | |
Trial protocol: ES (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2016-003819-36 | Sponsor Protocol Number: MK3475-586 | Start Date*: 2017-10-06 |
Sponsor Name:VU Medical Centre | ||
Full Title: Combining SBRT and pembrolizumab in early stage non-small cellular lungcancer patients planned for surgery: exploring safety and immunological proof of principle. | ||
Medical condition: Early stage (T1N0 and T2N0) non-small cell lung cancer | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Prematurely Ended) | ||
Trial results: (No results available) |
EudraCT Number: 2019-002721-30 | Sponsor Protocol Number: NIPU | Start Date*: 2021-01-14 | |||||||||||
Sponsor Name:Oslo University Hospital | |||||||||||||
Full Title: Nivolumab and ipilimumab +/- UV1 vaccination as second line treatment in patients with malignant mesothelioma (the NIPU-study) | |||||||||||||
Medical condition: Malignant pleural mesothelioma (MPM) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Trial now transitioned) ES (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-003064-47 | Sponsor Protocol Number: CUDC-101-104 | Start Date*: 2012-12-11 | |||||||||||
Sponsor Name:Curis, Inc. | |||||||||||||
Full Title: A Phase 1 open-label study to investigate the pharmacodynamics, metabolomics and pharmacokinetics of CUDC-101 in subjects with HER2 positive invasive breast cancer. | |||||||||||||
Medical condition: HER2 positive breast cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: GB (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-004190-12 | Sponsor Protocol Number: MK8808-003 | Start Date*: 2013-03-29 | |||||||||||
Sponsor Name:Merck Sharp & Dohme Corp., a subsidiary of Merck & Co., Inc. | |||||||||||||
Full Title: Randomized, Double-blind, Multicenter Study to Evaluate the Efficacy and Safety of MK-8808 versus MabThera™ in Patients with Advanced CD20-Positive Follicular Lymphoma. | |||||||||||||
Medical condition: Previously untreated patients with CD20-positive follicular lymphoma, Grade 1, 2 or 3a according to the WHO 2008 classification system. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2021-002672-40 | Sponsor Protocol Number: SGNTUC-029 | Start Date*: 2022-09-20 | |||||||||||||||||||||
Sponsor Name:Seagen Inc. | |||||||||||||||||||||||
Full Title: An Open-label Randomized Phase 3 Study of Tucatinib in Combination with Trastuzumab and mFOLFOX6 versus mFOLFOX6 given with or without either Cetuximab or Bevacizumab as First-line Treatment for Su... | |||||||||||||||||||||||
Medical condition: unresectable or metastatic HER2+ colorectal cancer | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: NO (Ongoing) SK (Ongoing) DE (Ongoing) ES (Ongoing) IT (Ongoing) FR (Ongoing) HU (Ongoing) IE (Ongoing) PT (Ongoing) BE (Ongoing) PL (Ongoing) AT (Ongoing) GR (Ongoing) NL (Ongoing) | |||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-000306-70 | Sponsor Protocol Number: 2009/07 | Start Date*: 2008-01-29 | |||||||||||
Sponsor Name:University of Dundee | |||||||||||||
Full Title: The effect of metformin on biomarker activity in primary breast cancer | |||||||||||||
Medical condition: Women with histologically proven operable primary, invasive breast cancer of ≥ 1cm in size. The study will involve women from the east of Scotland. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2021-002323-38 | Sponsor Protocol Number: GBG105GeparPiPPa | Start Date*: 2022-08-29 |
Sponsor Name:German Breast Group | ||
Full Title: A randomized, open-label, phase II trial comparing neoadjuvant endocrine therapy in combination with trastuzumab, pertuzumab +/- the PI3K inhibitor inavolisib in patients with HER2-positive, HR-pos... | ||
Medical condition: Patients with early breast cancer | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: DE (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2011-004126-10 | Sponsor Protocol Number: GO27983 | Start Date*: 2012-04-19 | |||||||||||
Sponsor Name:Genentech Inc. | |||||||||||||
Full Title: A PHASE Ib/II STUDY OF GDC-0068 OR GDC-0980 WITH ABIRATERONE ACETATE VERSUS ABIRATERONE ACETATE IN PATIENTS WITH CASTRATION-RESISTANT PROSTATE CANCER PREVIOUSLY TREATED WITH DOCETAXEL-BASED CHEMOTH... | |||||||||||||
Medical condition: Castration-Resistant Prostate Cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male | ||||||||||||
Trial protocol: GR (Completed) CZ (Completed) ES (Completed) GB (GB - no longer in EU/EEA) NL (Completed) FR (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-004752-77 | Sponsor Protocol Number: 20070820 | Start Date*: 2009-03-18 | |||||||||||
Sponsor Name:Amgen Inc | |||||||||||||
Full Title: A Phase 2 Study of Panitumumab Plus Irinotecan Followed by Panitumumab Plus AMG 479 in Subjects With Metastatic Colorectal Carcinoma Expressing Wild Type KRAS and Refractory to Oxaliplatin- or Irin... | |||||||||||||
Medical condition: Metastatic colorectal cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) FR (Completed) ES (Completed) IT (Completed) BE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-004714-41 | Sponsor Protocol Number: GBG69 | Start Date*: 2012-05-18 | |||||||||||
Sponsor Name:GBG Forschungs GmbH | |||||||||||||
Full Title: A randomized phase III trial comparing nanoparticle-based paclitaxel with solvent-based paclitaxel as part of neoadjuvant chemotherapy for patients with early breast cancer (GeparSepto) | |||||||||||||
Medical condition: Patients with primary breast cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2016-002480-34 | Sponsor Protocol Number: BH39147 | Start Date*: 2017-05-30 | |||||||||||
Sponsor Name:F. Hoffmann-La Roche Ltd | |||||||||||||
Full Title: A PHASE Ib/II STUDY EVALUATING THE SAFETY AND EFFICACY OF OBINUTUZUMAB IN COMBINATION WITH IDASANUTLIN AND VENETOCLAX IN PATIENTS WITH RELAPSED OR REFRACTORY FOLLICULAR LYMPHOMA AND OBINUTUZUMAB OR... | |||||||||||||
Medical condition: Relapsed or refractory (R/R) follicular lymphoma (FL) or diffuse large B-cell lymphoma (DLBCL). | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-000619-14 | Sponsor Protocol Number: GBG84 | Start Date*: 2014-11-04 |
Sponsor Name:German Breast Group | ||
Full Title: A randomized phase III trial comparing two dose-dense, dose-intensified approaches (ETC and PM(Cb)) for neoadjuvant treatment of patients with high-risk early breast cancer (GeparOcto) | ||
Medical condition: Patients with primary breast cancer | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Female | |
Trial protocol: DE (Completed) | ||
Trial results: View results |
EudraCT Number: 2018-003612-45 | Sponsor Protocol Number: A9001502 | Start Date*: 2019-09-06 |
Sponsor Name:Pfizer Inc. | ||
Full Title: TREATMENT RESISTANCE FOLLOWING ANTI-CANCER THERAPIES (TRANSLATE) | ||
Medical condition: Cancer | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: AT (Prematurely Ended) ES (Prematurely Ended) | ||
Trial results: View results |
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