- Trials with a EudraCT protocol (307)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (1)
307 result(s) found for: Stomach cancer.
Displaying page 1 of 16.
EudraCT Number: 2011-004405-25 | Sponsor Protocol Number: HIPEC_Stomach | Start Date*: 2012-03-01 | ||||||||||||||||
Sponsor Name:University Hospital Tübingen | ||||||||||||||||||
Full Title: Study for prevention of peritoneal carcinomatosis in patients with stomach cancer | ||||||||||||||||||
Medical condition: Reducing the risk of peritoneal carcinomatosis in patients with stomach cancer with following treatment: gastrectomy incl. HIPEC vs. gastrectomy excl. HIPEC | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: DE (Prematurely Ended) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2010-022164-12 | Sponsor Protocol Number: TOG301 | Start Date*: 2012-01-23 | ||||||||||||||||
Sponsor Name:Genta Incorporated | ||||||||||||||||||
Full Title: A randomized, double-blind study of capecitabine plus tesetaxel versus capecitabine plus placebo as second-line therapy in subjects with gastric cancer | ||||||||||||||||||
Medical condition: Histologically or cytologically confirmed gastric carcinoma, including gastric or gastroesophageal-junction adenocarcinoma | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: DE (Prohibited by CA) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-002321-30 | Sponsor Protocol Number: 12.01 | Start Date*: 2012-11-01 | |||||||||||
Sponsor Name:Odense University Hospital | |||||||||||||
Full Title: Randomized phase II trial with irinotecan as monotherapy compared to irinotecan and bevacizumab (BevIri) for patietns with platinum resistant non-resectable esophagus-, cardia or gastric cancer | |||||||||||||
Medical condition: Patients with esophagus or gastric cancer and who are platinum resistant and non-resectabel | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-020189-37 | Sponsor Protocol Number: IRST151.01 | Start Date*: 2010-08-13 | |||||||||||
Sponsor Name:ISTITUTO SCIENTIFICO ROMAGNOLO PER LO STUDIO E LA CURA DEI TUMORI | |||||||||||||
Full Title: A randomised phase II study of pre-operative or peri-operative docetaxel, oxaliplatin, capecitabine (DOX) regimen in patients with locally advanced resectable gastric cancer | |||||||||||||
Medical condition: Patient with potentially resectable adenocarcinoma of the stomach | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2010-022699-30 | Sponsor Protocol Number: B-DOCT | Start Date*: 2011-01-19 | |||||||||||||||||||||
Sponsor Name:Nederlands Kanker Instutuut-Antonie van Leeuwenhoek Ziekenhuis | |||||||||||||||||||||||
Full Title: Phase II Study of Docetaxel, Oxaliplatin, Capecitabine with Bevacizumab and Trastuzumab in case of human epidermal growth factor receptor 2 (HER2)-positivity in Patients with Locally Advanced or Me... | |||||||||||||||||||||||
Medical condition: Locally Advanced or Metastatic Gastric Cancer or Adenocarcinoma of the Gastro-oesophageal Junction | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: NL (Ongoing) | |||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-005046-37 | Sponsor Protocol Number: COUGAR-02 | Start Date*: 2007-12-28 | ||||||||||||||||
Sponsor Name:Cambridge University Hospitals NHS Foundation Trust | ||||||||||||||||||
Full Title: COUGAR-02: A randomised phase III study of docetaxel vs active symptom control in patients with relapsed oesophago-gastric adenocarcinoma | ||||||||||||||||||
Medical condition: Advanced oesophago-gastric cancer which has previously been treated with a platinum and fluoropyrimidine based combination | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: GB (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2004-004072-37 | Sponsor Protocol Number: 77/2004/O/Sper | Start Date*: 2004-09-09 | |||||||||||
Sponsor Name:AZIENDA OSPEDALIERA DI BOLOGNA POLICLINICO S. ORSOLA M. MALPIGHI | |||||||||||||
Full Title: CETUXIMAB AND FOLFIRI AS FIRST-LINE TREATMENT OF LOCALLY ADVANCED AND METASTATIC GASTRIC CANCER | |||||||||||||
Medical condition: Locally advanced or metastatic non-resectable gastric cancer stomach or gastro-esophageal junction | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-001500-36 | Sponsor Protocol Number: 27/2006/O/Sper | Start Date*: 2006-05-12 | |||||||||||
Sponsor Name:AZIENDA OSPEDALIERA DI BOLOGNA POLICLINICO S. ORSOLA M. MALPIGHI | |||||||||||||
Full Title: Radio-controlled surgery RGS in the gastric carcinoma locally advanced subordinate to neoadiuvante medical therapy. Clinical study of feasibilities and correlation with the traditional methodica... | |||||||||||||
Medical condition: carcinoma of the locally advanced stomach | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-006088-22 | Sponsor Protocol Number: Gastripec-I | Start Date*: 2011-03-28 | ||||||||||||||||
Sponsor Name:Klinik für Chirurgie, Charité Campus Virchow-Klinikum | ||||||||||||||||||
Full Title: Prospective multicenter phase III clinical trial using cytoreductive surgery with hyperthermic intraoperative chemotherapy (HIPEC) after preoperative chemotherapy in patients with peritoneal carc... | ||||||||||||||||||
Medical condition: Peritoneal carcinomatosis of gastric cancer incl. adenocarcinoma of the esophagogastreal junction | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: DE (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2006-004512-43 | Sponsor Protocol Number: ML20777 | Start Date*: 2007-01-29 | |||||||||||
Sponsor Name:Roche Farma, S.A. | |||||||||||||
Full Title: Estudio Fase II abierto de Capecitabina (Xeloda®) como fluoropirimidina de elección en combinación con quimioterapia en pacientes con cáncer gástrico Avanzado y/o Metastático susceptibles de ser tr... | |||||||||||||
Medical condition: Capecitabine in combination with chemotherapy in patients with advanced and/or metastatic gastric cancer suitable to be treated with a fluoropirimidine based regimen to assess the safety profile sp... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-006168-12 | Sponsor Protocol Number: 08.14 | Start Date*: 2008-11-17 | |||||||||||
Sponsor Name:Odense University Hospital | |||||||||||||
Full Title: Phase II trial with Cetuximab and Irinotecan (CetIri) for patients with platinum resistant esofagus- or gastric cancer | |||||||||||||
Medical condition: Patients with esofagus- and gastric cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-004223-27 | Sponsor Protocol Number: GEMCAD-0802 | Start Date*: 2008-10-29 | |||||||||||
Sponsor Name:GEMCAD | |||||||||||||
Full Title: Estudio fase II, de la combinación de Oxaliplatino y Sorafenib en pacientes con Adenocarcinoma gástrico o de la unión gastroesofágica localmente avanzado o metastásico, en progresión tras un esque... | |||||||||||||
Medical condition: CANCER GASTRICO | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-004504-39 | Sponsor Protocol Number: AIO STO-0601 | Start Date*: 2008-06-24 | |||||||||||
Sponsor Name:Martin-Luther-Universität Halle-Wittenberg, vertreten durch den Kanzler | |||||||||||||
Full Title: | |||||||||||||
Medical condition: | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2005-005464-92 | Sponsor Protocol Number: DOCOX-C-00082 | Start Date*: 2006-06-07 | |||||||||||
Sponsor Name:Sanofi-aventis groupe | |||||||||||||
Full Title: Estudio randomizado de fase II de Docetaxel en combinación con Oxaliplatino con o sin 5-FU o Capecitabina, en cáncer gástrico metastásico o en recurrencia local que no haya sido tratado previamente... | |||||||||||||
Medical condition: Cáncer gástrico metastásico o en recurrencia local que no haya sido tratado previamente para la enfermedad avanzada con quimioterapia | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) BE (Completed) GB (Completed) DE (Completed) HU (Completed) PT (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2016-002331-16 | Sponsor Protocol Number: PRODIGE51 | Start Date*: 2016-10-03 | |||||||||||||||||||||
Sponsor Name:Fédération Francophone de Cancérologie Digestive | |||||||||||||||||||||||
Full Title: | |||||||||||||||||||||||
Medical condition: | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: FR (Trial now transitioned) | |||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-006544-20 | Sponsor Protocol Number: CRAD001R2301 | Start Date*: 2009-07-06 | |||||||||||
Sponsor Name:Novartis Pharma Services AG | |||||||||||||
Full Title: A randomized, double-blind, multi-center phase III study comparing everolimus (RAD001) plus best supportive care versus placebo plus best supportive care in patients with advanced gastric cancer af... | |||||||||||||
Medical condition: advanced gastric cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Completed) BE (Completed) DE (Completed) GB (Completed) FR (Completed) IT (Completed) ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-016468-35 | Sponsor Protocol Number: D8480C00067 | Start Date*: 2016-03-29 | |||||||||||||||||||||||||||||||||||||||||
Sponsor Name:AstraZeneca AB | |||||||||||||||||||||||||||||||||||||||||||
Full Title: A randomised, double-blind, phase III efficacy and safety study of cediranib (RECENTIN™ ) when added to cisplatin plus a fluoropyrimidine, compared with cisplatin plus a fluoropyrimidine alone, in ... | |||||||||||||||||||||||||||||||||||||||||||
Medical condition: Gastric cancer | |||||||||||||||||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||||||||||||||||||||||
Trial protocol: GR (Completed) HU (Prematurely Ended) | |||||||||||||||||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2006-001503-10 | Sponsor Protocol Number: 29/2006/O/Sper | Start Date*: 2006-05-12 | |||||||||||
Sponsor Name:AZIENDA OSPEDALIERA DI BOLOGNA POLICLINICO S. ORSOLA M. MALPIGHI | |||||||||||||
Full Title: Technology of the radioisotopes for the intra-operative identification of the sentinel node in the premature gastric cancer. Clinical study of feasibility in order to improve the treatment and prog... | |||||||||||||
Medical condition: gastric cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-004130-32 | Sponsor Protocol Number: CRITICS | Start Date*: 2006-10-17 | |||||||||||
Sponsor Name:NKI/Antoni van Leeuwenhoek Ziekenhuis | |||||||||||||
Full Title: A multicenter randomized phase III trial of neo-adjuvant chemotherapy followed by surgery and chemotherapy or by surgery and chemoradiotherapy in resectable gastric cancer (CRITICS-study: ChemoRadi... | |||||||||||||
Medical condition: Resectable gastric cancer | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Ongoing) SE (Completed) DK (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-014895-23 | Sponsor Protocol Number: #0038 | Start Date*: 2013-02-01 | |||||||||||
Sponsor Name:Universitätsklinikum Erlangen | |||||||||||||
Full Title: Phase II clinical trial of a sequential therapy involving the FLOT regiment in palliative first-line treatment followed by AIO plus irinotecan in second-line treatment combined with supportive pare... | |||||||||||||
Medical condition: Advanced non-resectable adenocarcinoma of the stomach and the gastro-oesophageal junction | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
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