- Trials with a EudraCT protocol (36)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
36 result(s) found for: Hepatobiliary neoplasms.
Displaying page 1 of 2.
| EudraCT Number: 2018-003902-14 | Sponsor Protocol Number: EORTC-1741-GITCG | Start Date*: Information not available in EudraCT | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Sponsor Name:European Organisation for Research and Treatment of Cancer | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Full Title: DKN-01/atezolizumab as second line treatment of biliarY tract cancer and in combiNAtion or not with paclitaxel as second line treatMent of esophagogastrIC cancer: a multi-center Phase II Trial | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Medical condition: Non-operable biliary tract cancer (BTC) and non-operable esophagogastric cancer (EGC) adenocarcinoma. | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Trial protocol: CY (Prematurely Ended) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Trial results: (No results available) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| EudraCT Number: 2007-003056-12 | Sponsor Protocol Number: D4200L00007 | Start Date*: 2008-05-23 | |||||||||||
| Sponsor Name:ASTRAZENECA | |||||||||||||
| Full Title: A RANDOMISED, MULTICENTRE, PHASE II, PARALLEL-GROUP TRIAL OF VANDETANIB MONOTHERAPY OR VANDETANIB IN COMBINATION WITH GEMCITABINE VERSUS GEMCITABINE PLUS VANDETANIB MATCHING PLACEBO IN SUBJECTS WIT... | |||||||||||||
| Medical condition: ADVANCED BILIARY TRACT CANCER | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2010-023978-39 | Sponsor Protocol Number: 20080261 | Start Date*: 2011-05-23 | |||||||||||
| Sponsor Name:Amgen Inc | |||||||||||||
| Full Title: A Phase 2, Multicenter, Randomized, Double-blind, Placebo-controlled, Trial of AMG 479 or Placebo in Combination with Gemcitabine as First-line Therapy for Locally Advanced Unresectable Adenocarcin... | |||||||||||||
| Medical condition: Locally advanced adenocarcinoma of the pancreas | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DK (Prematurely Ended) GB (Prematurely Ended) DE (Prematurely Ended) PT (Prematurely Ended) BE (Prematurely Ended) AT (Prematurely Ended) CZ (Completed) PL (Prematurely Ended) SE (Prematurely Ended) HU (Completed) ES (Prematurely Ended) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2008-008652-16 | Sponsor Protocol Number: BR1-129 | Start Date*: 2009-10-01 | |||||||||||
| Sponsor Name:BRACCO IMAGING | |||||||||||||
| Full Title: QUANTITATIVE EVALUATION OF SONOVUE ENHANCED ULTRASONOGRAPHY FOR EARLY IDENTIFICATION OF SUBJECTS WITH HEPATOCELLULAR CARCINOMA REFRACTORY TO SORAFENIB THERAPY : A PHASE II EXPLORATIVE, INTRA-PATIEN... | |||||||||||||
| Medical condition: HCC epatocellular carcinoma | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Prematurely Ended) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2009-017428-17 | Sponsor Protocol Number: 20091105 | Start Date*: 2010-05-31 | ||||||||||||||||||||||||||
| Sponsor Name:AZIENDA OSPEDALIERA ORDINE MAURIZIANO | ||||||||||||||||||||||||||||
| Full Title: A Phase II Randomized Clinical Trial of Panitumumab plus Gemcitabine and Oxaliplatin (GEMOX) versus GEMOX alone as First Line Treatment in Advanced Biliary Tract Adenocarcinoma | ||||||||||||||||||||||||||||
| Medical condition: advanced intrahepatic colangiocarcinoma and extrahepatic biliary adenocarcinoma including gallbladder | ||||||||||||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
| Trial protocol: IT (Completed) | ||||||||||||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||||||||||||
| EudraCT Number: 2018-003833-14 | Sponsor Protocol Number: GOIRC-05-2018 | Start Date*: 2019-03-21 | ||||||||||||||||
| Sponsor Name:GRUPPO ONCOLOGICO ITALIANO DI RICERCA CLINICA (GOIRC) | ||||||||||||||||||
| Full Title: A Phase IV study on impact of Edoxaban treatment in Italian cancer patients with venous thromboembolism (EDOI Cancer Study) during antineoplastic therapy | ||||||||||||||||||
| Medical condition: Venous thromboembolism event associated with cancer | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: IT (Completed) | ||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||
| EudraCT Number: 2017-003323-30 | Sponsor Protocol Number: EORTC-1607-GITCG | Start Date*: 2020-01-20 | |||||||||||||||||||||||||||||||
| Sponsor Name:European Organisation for the Research and Treatment of Cancer (EORTC) | |||||||||||||||||||||||||||||||||
| Full Title: Open-label first line, single-arm phase II study of CisGem combined with pembrolizumab in patients with advanced or metastatic biliary tract cancer | |||||||||||||||||||||||||||||||||
| Medical condition: Non-resectable or recurrent/metastatic BTC | |||||||||||||||||||||||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||||||||||||||||||||||
| Trial protocol: GB (GB - no longer in EU/EEA) ES (Ongoing) | |||||||||||||||||||||||||||||||||
| Trial results: View results | |||||||||||||||||||||||||||||||||
| EudraCT Number: 2009-014293-17 | Sponsor Protocol Number: AGO/2009/006 | Start Date*: 2009-09-10 | |||||||||||
| Sponsor Name:University Hospital Ghent | |||||||||||||
| Full Title: Phase II study of cetuximab combined with cisplatin or carboplatin/pemetrexed as first line treatment in patients with malignant pleural mesothelioma. | |||||||||||||
| Medical condition: Patients with malignant pleural mesothelioma | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: BE (Completed) NL (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2011-006194-26 | Sponsor Protocol Number: EC11-185 | Start Date*: 2012-06-29 | |||||||||||
| Sponsor Name:JOSE LUIS MONTERO ALVAREZ | |||||||||||||
| Full Title: A phase IV, multicenter, randomized, double-blind, placebo-controlled study of efficacy and safety of Sorafenib in patients with hepatocellular carcinoma after radiological progression | |||||||||||||
| Medical condition: Advanced stage hepatocellular carcinoma (stage C of BCLC classification) | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: ES (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2011-005909-79 | Sponsor Protocol Number: PRIGA | Start Date*: 2012-04-12 | |||||||||||
| Sponsor Name:Fundació Clínic per a la Recerca Biomèdica | |||||||||||||
| Full Title: Magnetic resonance with gadoxetic acid for the diagnosis of hepatocellular carcinoma in patients with liver cirrhosis. Evaluation of its impact for the non-invasive diagnosis. | |||||||||||||
| Medical condition: hepatocellular carcinoma | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: ES (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2010-020398-18 | Sponsor Protocol Number: 20060540 | Start Date*: 2010-12-22 | ||||||||||||||||
| Sponsor Name:Amgen Inc. | ||||||||||||||||||
| Full Title: A Phase 3, Multicenter, Randomized, Double-Blind, Placebo Controlled, Trial of AMG 479 or Placebo in Combination with Gemcitabine as First-line Therapy for Metastatic Adenocarcinoma of the Pancreas | ||||||||||||||||||
| Medical condition: metastatic adenocarcinoma of the pancreas | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: FI (Prematurely Ended) NL (Prematurely Ended) HU (Completed) AT (Prematurely Ended) GB (Prematurely Ended) BE (Prematurely Ended) CZ (Completed) SE (Prematurely Ended) PT (Prematurely Ended) LT (Prematurely Ended) SK (Completed) DK (Prematurely Ended) GR (Prematurely Ended) DE (Prematurely Ended) SI (Prematurely Ended) IT (Prematurely Ended) BG (Prematurely Ended) ES (Prematurely Ended) | ||||||||||||||||||
| Trial results: View results | ||||||||||||||||||
| EudraCT Number: 2016-005175-27 | Sponsor Protocol Number: IB2017-01 | Start Date*: 2018-03-14 | ||||||||||||||||||||||||||
| Sponsor Name:Institut Bergonié | ||||||||||||||||||||||||||||
| Full Title: A phase I/II study of Regorafenib plus Avelumab in digestive tumors | ||||||||||||||||||||||||||||
| Medical condition: Adult patients with advanced or metastatic digestive solid tumors | ||||||||||||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
| Trial protocol: FR (Trial now transitioned) | ||||||||||||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||||||||||||
| EudraCT Number: 2018-001796-21 | Sponsor Protocol Number: 2102-ONC-102 | Start Date*: 2019-02-21 | |||||||||||||||||||||||||||||||
| Sponsor Name:Forma Therapeutics, Inc. | |||||||||||||||||||||||||||||||||
| Full Title: A Phase 1b/2 Study of FT-2102 in Patients with Advanced Solid Tumors and Gliomas with an IDH1 Mutation | |||||||||||||||||||||||||||||||||
| Medical condition: Advanced Solid Tumors and Gliomas with an IDH1 Mutation | |||||||||||||||||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||||||||||||
| Trial protocol: GB (GB - no longer in EU/EEA) FR (Completed) ES (Completed) | |||||||||||||||||||||||||||||||||
| Trial results: (No results available) | |||||||||||||||||||||||||||||||||
| EudraCT Number: 2019-002860-29 | Sponsor Protocol Number: ONC-2019-002 | Start Date*: 2019-12-12 | |||||||||||
| Sponsor Name:IRCCS ISTITUTO CLINICO HUMANITAS | |||||||||||||
| Full Title: Efficacy and safety of Cabozantinib in patients with hepatocellular carcinoma progressing on or intolerant to prior treatment with immune checkpoint inhibitors: A Phase II study (Immunocabo). | |||||||||||||
| Medical condition: Hepatocellular carcinoma (HCC) | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Trial now transitioned) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2012-002128-33 | Sponsor Protocol Number: 004-IRCC-10IIS-12 | Start Date*: 2012-05-29 | |||||||||||
| Sponsor Name:FONDAZIONE DEL PIEMONTE PER L'ONCOLOGIA IRCC DI CANDIOLO | |||||||||||||
| Full Title: Open-Label, Phase II Study of Trastuzumab in Combination with Lapatinib or Pertuzumab in Combination with Trastuzumab in Patients with HER2-positive Metastatic Colorectal Cancer: the HERACLES Trial... | |||||||||||||
| Medical condition: Metastatic colorectal carcinoma (mCRC) | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2011-002149-36 | Sponsor Protocol Number: G-202-002 | Start Date*: 2012-12-10 | |||||||||||
| Sponsor Name:GenSpera, Inc. | |||||||||||||
| Full Title: An Open-Label, Single-Arm, Phase 2 Study of G-202 in Patients with Chemotherapy-Naïve Metastatic Castrate-Resistant Prostate Cancer | |||||||||||||
| Medical condition: chemotherapy-naïve metastatic castrate-resistant prostate cancer | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male | ||||||||||||
| Trial protocol: GB (Prematurely Ended) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2019-004953-96 | Sponsor Protocol Number: JTX-4014-202 | Start Date*: 2020-06-24 | |||||||||||
| Sponsor Name:Jounce Therapeutics, Inc. | |||||||||||||
| Full Title: Phase 2 Study of PD-1 Inhibitor JTX-4014 Alone and in Combination with Vopratelimab, an ICOS Agonist, in Biomarker-selected Subjects with Metastatic NSCLC After One Prior Platinum-containing Regimen | |||||||||||||
| Medical condition: Metastatic Non Small Cell Lung Cancer (NSCLC) | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: HU (Completed) SK (Completed) BG (Completed) HR (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2016-004118-84 | Sponsor Protocol Number: ONC-2016-001 | Start Date*: 2017-04-21 | |||||||||||
| Sponsor Name:IRCCS ISTITUTO CLINICO HUMANITAS | |||||||||||||
| Full Title: A multicenter, phase I-II trial of gemcitabine plus oxaliplatin and nbb-paclitaxel in subjects with advanced (unresectable or metastatic) biliary tract cancer (gallbladder cancer, cancer of the ext... | |||||||||||||
| Medical condition: Advanced (unresectable or metastatic) biliary tract cancer | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2010-021598-35 | Sponsor Protocol Number: UCL/08/0255 | Start Date*: 2010-08-26 | |||||||||||
| Sponsor Name:University College London | |||||||||||||
| Full Title: Phase II study of Bortezomib, Adriamycin and Dexamethasone (PAD) therapy for previously untreated patients with multiple myeloma: Impact of minimal residual disease (MRD) in patients with deferred ... | |||||||||||||
| Medical condition: Multiple Myeloma | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2018-004186-14 | Sponsor Protocol Number: CORT125134-552 | Start Date*: 2019-07-31 | |||||||||||||||||||||
| Sponsor Name:Corcept Therapeutics Incorporated | |||||||||||||||||||||||
| Full Title: A Phase 2, Randomized, Open-label, 3-arm Study of Relacorilant in Combination with Nab-Paclitaxel for Patients with Platinum Resistant Ovarian, Fallopian Tube, or Primary Peritoneal Cancer | |||||||||||||||||||||||
| Medical condition: Recurrent Platinum-Resistant Ovarian, Fallopian Tube, or Primary Peritoneal Cancer | |||||||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Female | ||||||||||||||||||||||
| Trial protocol: BE (Completed) ES (Ongoing) IT (Completed) | |||||||||||||||||||||||
| Trial results: View results | |||||||||||||||||||||||
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