- Trials with a EudraCT protocol (1,473)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
1,473 result(s) found for: Cancer biomarkers.
Displaying page 1 of 74.
EudraCT Number: 2018-002101-65 | Sponsor Protocol Number: PI17/01109 | Start Date*: 2018-11-19 | |||||||||||
Sponsor Name:Ángel Lanas Arbeloa-Instituto de Investigación Sanitaria Aragón | |||||||||||||
Full Title: Assessment of direct biomarkers of aspirin action to develop a precision chemoprevention therapy of colorectal cancer | |||||||||||||
Medical condition: Colorectal cancer with a recent confirmed diagnosis (less than 48h) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2014-004513-90 | Sponsor Protocol Number: UMCN-AKF-14.07 | Start Date*: 2015-03-17 | |||||||||||
Sponsor Name:Radboud UMC | |||||||||||||
Full Title: Optimizing abiraterone (Zytiga®) therapy by exploring the relation between an early biomarker - drug exposure - as a predictor for drug response in patients with mCRPC (OPTIMUM - STUDY) | |||||||||||||
Medical condition: Metastatic Castration Resistant Prostate Cancer (mCRPC) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male | ||||||||||||
Trial protocol: NL (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-004226-82 | Sponsor Protocol Number: 10077 | Start Date*: 2006-09-07 | |||||||||||
Sponsor Name:University Hospitals of Leicester NHS Trust | |||||||||||||
Full Title: PHARMACODYNAMIC STUDY OF ORAL MIRTOSELECT IN PATIENTS WITH SUSPECTED COLORECTAL DISEASE | |||||||||||||
Medical condition: Patients with operable colorectal cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-002686-30 | Sponsor Protocol Number: CEP-AZ-SH-02 | Start Date*: 2009-04-15 | |||||||||||
Sponsor Name:Christie Hospital NHS Foundation Trust | |||||||||||||
Full Title: Assessment of the effects of the specific endothelin-A antagonist ZD4054 on prostate cancer biomarkers in patients with castrate-resistant metastatic disease | |||||||||||||
Medical condition: Prostate cancer | |||||||||||||
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Population Age: | Gender: Male | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2015-000860-32 | Sponsor Protocol Number: UMCN-AKF-14.17 | Start Date*: 2015-04-28 | |||||||||||||||||||||
Sponsor Name:Radboud University Medical Center | |||||||||||||||||||||||
Full Title: Personalizing enzalutamide (Xtandi®) therapy by understanding the relation between the decrease in the expression profile of a panel of preselected microRNAs, tumor related mRNAs and treatment resp... | |||||||||||||||||||||||
Medical condition: Metastatic Castration Resistant Prostate Cancer (mCRPC) | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male | ||||||||||||||||||||||
Trial protocol: NL (Completed) | |||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2013-004139-62 | Sponsor Protocol Number: CRAD001JES13 | Start Date*: 2014-01-02 | |||||||||||
Sponsor Name:Novartis Farmacéutica S. A. | |||||||||||||
Full Title: A pilot open-label, phase II, single-arm study to evaluate the association of biomarkers of hormonal resistance and the mTOR pathway with the clinical efficacy of everolimus plus letrozole in the f... | |||||||||||||
Medical condition: Estrogen receptor or progesterone receptor positive locally advanced or metastatic breast cancer in postmenopausal women | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: ES (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2018-004458-14 | Sponsor Protocol Number: PROvING | Start Date*: 2020-11-05 | ||||||||||||||||||||||||||
Sponsor Name:AZIENDA OSPEDALIERO-UNIVERSITARIA PISANA | ||||||||||||||||||||||||||||
Full Title: Phase III clinical trial Oligometastatic and Oligorecurrent PROstate Cancer: enhancing patients’ selection by new ImagiNG biomarkers | ||||||||||||||||||||||||||||
Medical condition: Prostate cancer | ||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male | |||||||||||||||||||||||||||
Trial protocol: IT (Completed) | ||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-000662-23 | Sponsor Protocol Number: BO21015 | Start Date*: 2008-10-28 | |||||||||||
Sponsor Name:F. Hoffmann La-Roche Ltd | |||||||||||||
Full Title: A randomized, multicenter phase II study to explore whether biomarkers correlate with treatment outcome in chemo-naive patients with advanced or recurrent non-squamous non-small cell lung cancer, w... | |||||||||||||
Medical condition: Locally advanced, metastatic or recurrent Non-small Cell Lung Cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Completed) ES (Completed) HU (Completed) BE (Completed) DE (Completed) DK (Completed) CZ (Completed) IT (Completed) FR (Completed) GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2015-001001-14 | Sponsor Protocol Number: IEO240 | Start Date*: 2015-10-07 | |||||||||||
Sponsor Name:ISTITUTO EUROPEO DI ONCOLOGIA | |||||||||||||
Full Title: ¿A randomized placebo controlled phase II study with metformin in metabolic-unbalanced breast cancer survivors at higher risk for recurrence (MetBreCS)¿ | |||||||||||||
Medical condition: Metabolic-unbalanced breast cancer survivors at higher risk for recurrence (triple negative breast cancer, luminal B Her2 positive, non luminal HER2 positive) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: IT (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-011377-33 | Sponsor Protocol Number: 08_CLPHA_55 | Start Date*: 2009-06-25 | |||||||||||
Sponsor Name:The Christie NHS Foundation Trust | |||||||||||||
Full Title: AN ASSESSMENT OF IMAGING AND CIRCULATING BIOMARKERS IN PATIENTS WITH METASTATIC COLORECTAL CARCINOMA TREATED WITH THE ANTI-VEGF MONOCLONAL ANTIBODY BEVACIZUMAB | |||||||||||||
Medical condition: Metastatic colorectal cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-001661-32 | Sponsor Protocol Number: VeTo | Start Date*: 2012-07-05 | |||||||||||||||||||||
Sponsor Name:Vejle Hospital, Dept. of Oncology | |||||||||||||||||||||||
Full Title: Veliparib (ABT888) and Topotecan (Hycamtin®) for Patients with Platinum-Resistant or Partially Platinum-Sensitive Relapse of Epithelial Ovarian Cancer with Negative or Unknown BRCA Status | |||||||||||||||||||||||
Medical condition: Relapsed epithelial, platinum resistant ovarian cancer with negative or unknown BRCA status | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||||||||||||
Trial protocol: DK (Completed) | |||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2009-018148-45 | Sponsor Protocol Number: H3E-EW-JMIP | Start Date*: 2010-10-20 | ||||||||||||||||
Sponsor Name:Eli Lilly and Company Limited | ||||||||||||||||||
Full Title: An exploratory Phase 2 study of Pemetrexed and Cisplatin as Preoperative chemotherapy in the treatment of Stage IIIAN2 nonsquamous non-Small cell lung cancer | ||||||||||||||||||
Medical condition: Non Squamous Non Small Cell Lung Cancer | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: IT (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2011-005197-40 | Sponsor Protocol Number: I1D-MC-JIAE | Start Date*: 2012-07-20 | |||||||||||
Sponsor Name:Eli Lilly and Company | |||||||||||||
Full Title: A Randomized, Double-Blind, Placebo-Controlled Phase 1b/2 Study of LY2228820, a p38MAPK Inhibitor, plus Gemcitabine and Carboplatin versus Gemcitabine and Carboplatin for Women with Platinum-Sensit... | |||||||||||||
Medical condition: Epithelial ovarian cancer, fallopian tube cancer, and primary peritoneal cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: DE (Completed) BE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2019-000502-30 | Sponsor Protocol Number: DKFZ-2019-001 | Start Date*: 2020-03-26 | |||||||||||||||||||||
Sponsor Name:German Cancer Research Center (DKFZ) | |||||||||||||||||||||||
Full Title: Personalized Vitamin D Supplementation for Reducing or Preventing Fatigue and Enhancing Quality of Life of Patients with Colorectal Tumor: Randomized Intervention Trial | |||||||||||||||||||||||
Medical condition: Fatigue in patients with colorectal cancer (ICD codes C18-C20 and C21.8) within 12 months after a colorectal cancer therapy (surgery, chemotherapy and/ or radiation) and not optimal vitamin D status | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: DE (Trial now transitioned) | |||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2010-019384-11 | Sponsor Protocol Number: EFC10259 | Start Date*: Information not available in EudraCT | |||||||||||
Sponsor Name:sanofi-aventis recherche & développement | |||||||||||||
Full Title: A multinational, randomized, double blind, controlled phase II trial of ombrabulin with taxane and platinum combination administered every three weeks, in first line treatment of patients with meta... | |||||||||||||
Medical condition: Non-small cell lung cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-002755-15 | Sponsor Protocol Number: GM-IMAB-002-01 | Start Date*: 2014-01-28 | ||||||||||||||||
Sponsor Name:Ganymed Pharmaceuticals AG | ||||||||||||||||||
Full Title: A first-in-human dose escalation and dose finding phase I/II trial of IMAB027 in patients with recurrent advanced ovarian cancer | ||||||||||||||||||
Medical condition: recurrent advanced ovarian cancer | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Female | |||||||||||||||||
Trial protocol: BE (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2021-004061-13 | Sponsor Protocol Number: ESR21-21165 | Start Date*: 2022-06-09 | ||||||||||||||||
Sponsor Name:VHIO Vall d’Hebron Institute of Oncology | ||||||||||||||||||
Full Title: Single cell characterization of persistent cells upon treatment with durvalumab (MEDI4736) with or without tremelimumab in MSS and MSI colorectal and endometrial tumors | ||||||||||||||||||
Medical condition: MSS and MSI colorectal and endometrial tumors | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: ES (Ongoing) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-001395-74 | Sponsor Protocol Number: MER-101-03 | Start Date*: 2008-06-30 | |||||||||||
Sponsor Name:Merrion Pharmaceuticals plc | |||||||||||||
Full Title: A multi-center Phase II study to compare MER-101 20mg tablets to intravenous Zometa® 4mg in male bisphosphonate-naïve, hormone-refractory prostate cancer patients | |||||||||||||
Medical condition: Hormone - refractory prostate cancer with bone metastases and no prior bisphoshonate treatment | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male | ||||||||||||
Trial protocol: EE (Completed) LV (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2016-004120-39 | Sponsor Protocol Number: 1.0 | Start Date*: 2017-03-13 | |||||||||||
Sponsor Name:Region Skåne | |||||||||||||
Full Title: An experimental pilot study on immune and inflammatory biomarkers in patients with advanced prostatecancer treated with degarelix vs. GnRH agonist and with cardiovascular disease | |||||||||||||
Medical condition: Patients with advanced prostate cancer and pre-existing cardiovascular disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male | ||||||||||||
Trial protocol: SE (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-006323-31 | Sponsor Protocol Number: D1532C00016 | Start Date*: 2009-05-19 | |||||||||||||||||||||
Sponsor Name:AstraZeneca AB | |||||||||||||||||||||||
Full Title: D1532C00016: A Phase II, Double-Blind, Randomised, Placebo-Controlled Study to Assess the Efficacy of AZD6244 (Hyd-Sulfate) in Combination with Docetaxel, Compared with Docetaxel Alone, in 2nd Line... | |||||||||||||||||||||||
Medical condition: 2nd Line Patients with KRAS Mutation Positive Locally Advanced or Metastatic Non Small Cell Lung Cancer (Stage IIIB – IV) | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: HU (Completed) CZ (Completed) DK (Completed) ES (Completed) BE (Completed) FR (Completed) IT (Completed) BG (Completed) | |||||||||||||||||||||||
Trial results: View results |
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