- Trials with a EudraCT protocol (138)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
138 result(s) found for: Diet and cancer.
Displaying page 1 of 7.
EudraCT Number: 2019-004600-35 | Sponsor Protocol Number: 70880 | Start Date*: 2020-02-25 | |||||||||||
Sponsor Name:Department of Hepatology and Gastroenterology, Aarhus University Hospital | |||||||||||||
Full Title: Fat-reduced diet vs. bile acid binder as a treatment for bile acid malabsorption in patients with chronic diarrhoea as a late side effect after cancer treatment in the pelvic region - a randomised,... | |||||||||||||
Medical condition: Bile acid malabsorption as a late side effect to cancer treatment in the pelvic region. | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2004-000851-41 | Sponsor Protocol Number: DRI5029 | Start Date*: 2004-10-04 | |||||||||||
Sponsor Name:Sanofi-Synthelabo AB | |||||||||||||
Full Title: A randomized, double-blind, placebo-controlled, parallel-group, fixed-dose, multicenter study evaluating the efficacy and safety of four doses of SR147778 in obese patients | |||||||||||||
Medical condition: Obesity is becoming a major health problem in western societies. Its prevalence is increasing especially in USA, UK, and Germany. Obesity is responsible for increased morbidity and mortality. The c... | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: FI (Completed) ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-012007-25 | Sponsor Protocol Number: BAY43-9006/14295 | Start Date*: 2009-10-21 | |||||||||||||||||||||
Sponsor Name:Bayer AG | |||||||||||||||||||||||
Full Title: A Double-Blind, Randomized Phase III Study Evaluating the Efficacy and Safety of Sorafenib Compared to Placebo in Locally Advanced/Metastatic RAI-Refractory Differentiated Thyroid Cancer | |||||||||||||||||||||||
Medical condition: Differentiated thyroid cancer | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: DE (Completed) GB (Completed) ES (Completed) IT (Completed) NL (Completed) FR (Completed) DK (Completed) SE (Completed) BE (Completed) AT (Completed) SK (Completed) BG (Completed) | |||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2005-006111-47 | Sponsor Protocol Number: SC03005 | Start Date*: 2006-03-27 | |||||||||||
Sponsor Name:McNeil Ltd | |||||||||||||
Full Title: A double-blind, randomised, parallel group pilot study to compare macrogol 3350 + electrolytes versus placebo in the overnight relief of constipation | |||||||||||||
Medical condition: Constipation | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: IE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-005427-32 | Sponsor Protocol Number: MeMeMe | Start Date*: 2014-08-18 |
Sponsor Name:Fondazione IRCCS Istituto Nazionale dei Tumori | ||
Full Title: Randomized controlled trial of metformin and dietary restriction to prevent age-related morbid events in people with metabolic syndrome | ||
Medical condition: metabolic syndrome | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: IT (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2012-003226-25 | Sponsor Protocol Number: Abifood01 | Start Date*: 2013-07-12 | |||||||||||
Sponsor Name:Fundacion Publica Andaluza para la Gestion de la Investigacion en Salud de Sevilla | |||||||||||||
Full Title: Phase I, randomized, open design trial to evaluate the effect of food (fasting, fat meal and standard meal) on the pharmacokinetics of abiraterone acetate at reduced doses, compared with convention... | |||||||||||||
Medical condition: metastatic prostatic cancer after castration-resistant progression to docetaxel | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male | ||||||||||||
Trial protocol: ES (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2021-000845-42 | Sponsor Protocol Number: CBYL719A0HR01T | Start Date*: 2022-04-04 |
Sponsor Name:CCGCRO | ||
Full Title: Impact of time of alpelisib administration, concomitant fasting and low carbohydrate diet on alpelisib toxicity and efficacy; a pilot randomized controlled phase IIb trial - ITACA | ||
Medical condition: metastatic breast cancer HER2- HR+ PIK3CA+ | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: HR (Suspended by CA) | ||
Trial results: (No results available) |
EudraCT Number: 2019-003093-13 | Sponsor Protocol Number: BREAKFAST | Start Date*: 2020-01-14 | |||||||||||
Sponsor Name:FONDAZIONE IRCCS "ISTITUTO NAZIONALE DEI TUMORI" | |||||||||||||
Full Title: Targeting triple negative BREAst cancer metabolism with a combination of chemotherapy and a diet mimicking FASTing plus/minus metformin in the preoperative setting: the BREAKFAST trial | |||||||||||||
Medical condition: Targeting triple negative BREAst cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: IT (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-012787-14 | Sponsor Protocol Number: BAY73-4506/14387 | Start Date*: 2010-05-10 | ||||||||||||||||||||||||||
Sponsor Name:Bayer HealthCare AG | ||||||||||||||||||||||||||||
Full Title: A randomized, double-blind, placebo-controlled phase III study of regorafenib plus BSC versus placebo plus BSC in patients with metastatic colorectal cancer (CRC) who have progressed after standar... | ||||||||||||||||||||||||||||
Medical condition: Metastatic Colorectal Carcinoma | ||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: BE (Completed) DE (Completed) HU (Completed) PT (Completed) ES (Completed) CZ (Completed) IT (Completed) FR (Completed) NL (Completed) | ||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2017-001634-26 | Sponsor Protocol Number: RPH001BEV01 | Start Date*: 2017-06-07 | |||||||||||
Sponsor Name:TRPHARM | |||||||||||||
Full Title: Phase I, Double Blind, Randomized, Parallel-Arm, Single-Dose, Pharmacokinetic and Safety Study of Bevacizumab-biosimilar (RPH-001) Compared to Bevacizumab-innovator (Avastin®, Roche) in Healthy Mal... | |||||||||||||
Medical condition: Non-Small Cell Lung Cancer | |||||||||||||
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Population Age: Adults | Gender: Male | ||||||||||||
Trial protocol: Outside EU/EEA | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2013-004108-20 | Sponsor Protocol Number: UMCN-AKF13.05 | Start Date*: 2014-03-17 | ||||||||||||||||
Sponsor Name:Radboud University Nijmegen Medical Centre | ||||||||||||||||||
Full Title: Improving the tolerability of the oral targeted anti-cancer drug pazopanib by food intake (DIET) | ||||||||||||||||||
Medical condition: Patients who are treated or will be treated with pazopanib. | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: NL (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2019-001219-22 | Sponsor Protocol Number: SGNTV-002 | Start Date*: 2019-10-25 | |||||||||||||||||||||
Sponsor Name:Seattle Genetics, Inc. | |||||||||||||||||||||||
Full Title: Open Label Phase 2 Study of Tisotumab Vedotin for Patients with Platinum-Resistant Ovarian Cancer with a Safety Run-in of a Dose-Dense Regimen | |||||||||||||||||||||||
Medical condition: Patients with epithelial ovarian cancer, primary peritoneal cancer, or fallopian tube cancer (hereafter collectively referred to as platinum-resistant ovarian cancer and abbreviated as PROC) | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||||||||||||
Trial protocol: ES (Prematurely Ended) IE (Prematurely Ended) BE (Completed) DK (Prematurely Ended) IT (Prematurely Ended) | |||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2017-003835-12 | Sponsor Protocol Number: AC17067 | Start Date*: 2018-03-01 | |||||||||||||||||||||
Sponsor Name:The University Of Edinburgh [...] | |||||||||||||||||||||||
Full Title: A placebo controlled randomised trial of intravenous lidocaine in accelerating gastrointestinal recovery after colorectal surgery | |||||||||||||||||||||||
Medical condition: Patients scheduled for elective colorectal resection for colorectal cancer or diverticular disease. | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) | |||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2011-002947-83 | Sponsor Protocol Number: 40085-75083 | Start Date*: 2013-04-26 | |||||||||||
Sponsor Name:European Organisation for Research and Treatment of Cancer | |||||||||||||
Full Title: Treatment of patients with KRAS wild type advanced colorectal cancer with 5-fluorouracil (5-FU) or 5-FU plus an Epidermal Growth Factor Receptor inhibitor (cetuximab) based on a Comprehensive Geria... | |||||||||||||
Medical condition: Metastatic Colorectal Cancer | |||||||||||||
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Population Age: Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) BE (Completed) ES (Prematurely Ended) GB (Prematurely Ended) IT (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2014-001436-10 | Sponsor Protocol Number: INCB18424-266 | Start Date*: 2015-02-26 | |||||||||||||||||||||||||||||||
Sponsor Name:Incyte Corporation | |||||||||||||||||||||||||||||||||
Full Title: A Randomized, Double-Blind Phase 2 Study of Ruxolitinib or Placebo in Combination With Pemetrexed/Cisplatin and Pemetrexed Maintenance for Initial Treatment of Subjects With Nonsquamous Non–Small C... | |||||||||||||||||||||||||||||||||
Medical condition: Nonsquamous NSCLC that is Stage IIIB, Stage IV, or recurrent | |||||||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||||||||||||
Trial protocol: IT (Completed) DK (Prematurely Ended) ES (Prematurely Ended) NL (Completed) PT (Completed) | |||||||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2011-002185-21 | Sponsor Protocol Number: 11GS005 | Start Date*: 2011-09-15 | |||||||||||
Sponsor Name:Research and Development Nottingham University Hospital | |||||||||||||
Full Title: An open label study to determine the efficacy of ferric carboxymaltose in preoperative colorectal cancer related anaemia, and to develop biomarkers to predict response to this treatment strategy | |||||||||||||
Medical condition: The medical condition to be investigated is anaemia (low blood count) in pre-operative patients with colorectal cancer. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2022-003713-11 | Sponsor Protocol Number: 1938/2022 | Start Date*: 2023-11-17 |
Sponsor Name:Medical University of Vienna [...] | ||
Full Title: [177Lu]Lu-PSMAI&T radioligand therapy (PSMA-RLT) for patients with prostate cancer and biochemical but not radio-morphological local recurrence after primary therapy with curative intent: A Prospec... | ||
Medical condition: Prostate cancer | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male | |
Trial protocol: AT (Trial now transitioned) | ||
Trial results: (No results available) |
EudraCT Number: 2011-001468-23 | Sponsor Protocol Number: TG4010.14 | Start Date*: 2011-12-19 | ||||||||||||||||
Sponsor Name:Transgene S.A. | ||||||||||||||||||
Full Title: A Phase IIb/III randomized, double-blind, placebo-controlled study comparing first-line therapy with or without TG4010 immunotherapy product in patients with stage IV non-small cell lung cancer (NS... | ||||||||||||||||||
Medical condition: Stage IV non small cell lung cancer (NSCLC) | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: BE (Completed) HU (Completed) GB (Completed) DE (Prematurely Ended) ES (Completed) PL (Completed) IT (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2016-003036-20 | Sponsor Protocol Number: 1-2016 | Start Date*: 2017-10-02 | |||||||||||
Sponsor Name:FONDAZIONE IRCCS "ISTITUTO NAZIONALE DEI TUMORI" | |||||||||||||
Full Title: A randomized trial of multifactorial primary prevention in high risk subjects candidate to a lung cancer early detection CT program | |||||||||||||
Medical condition: health subjects (multifactorial primary prevention) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2018-003249-41 | Sponsor Protocol Number: M18DMB | Start Date*: 2018-12-06 |
Sponsor Name:Modra Pharmaceuticals B.V. | ||
Full Title: A multicentre phase IIa study to evaluate the efficacy and tolerability of ModraDoc006/r in patients with recurrent or metastatic HER-2 negative breast cancer, suitable for treatment with a taxane | ||
Medical condition: recurrent/ metastatic HER-2 negative breast cancer, suitable for treatment with a taxane | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Female | |
Trial protocol: BE (Completed) DK (Completed) ES (Ongoing) | ||
Trial results: View results |
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