- Trials with a EudraCT protocol (43)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
43 result(s) found for: Gall bladder disease.
Displaying page 2 of 3.
EudraCT Number: 2020-005832-31 | Sponsor Protocol Number: ALXN1840-HV-Cu-Absorption | Start Date*: 2021-04-13 | |||||||||||
Sponsor Name:Alexion Pharmaceuticals Inc. | |||||||||||||
Full Title: Efficacy of ALXN1840 on human hepatic copper uptake quantified with 64CuCl2 PET/CT-scan. | |||||||||||||
Medical condition: Healthy Volunteers (Wilson's disease) | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2020-005007-40 | Sponsor Protocol Number: MK-6482-016 | Start Date*: 2021-08-10 | |||||||||||
Sponsor Name:Merck Sharp & Dohme Corp., a subsidiary of Merck & Co., Inc. | |||||||||||||
Full Title: An Open-label, Multicenter, Phase 2 Study to Evaluate the Efficacy and Safety of Pembrolizumab Plus Lenvatinib in Combination With Belzutifan in Multiple Solid Tumors | |||||||||||||
Medical condition: HCC, non-microsatellite instability-high (MSI-H)/ deficient mismatch repair (dMMR) CRC, PDAC, and BTC | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Trial now transitioned) ES (Ongoing) FR (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2013-001364-30 | Sponsor Protocol Number: BBH-TQL-LC | Start Date*: 2013-07-22 | |||||||||||
Sponsor Name:Bispebjerg Hospital | |||||||||||||
Full Title: Ultrasoundguided transmuscular quadrates lumborum block after elective laparoscopic cholecystectomy. A prospective, randomised clinical trial. | |||||||||||||
Medical condition: Postoperative pain following laparoscopic cholecystectomy | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2010-020188-19 | Sponsor Protocol Number: 1003 | Start Date*: 2010-09-24 | |||||||||||
Sponsor Name:Oncology Department | |||||||||||||
Full Title: Intra-hepatic chemotherapy with oxaliplatin every second week in combination with systemic gemcitabine and capecitabine and in patients with a KRAS-wild type tumour in combination with cetuximab in... | |||||||||||||
Medical condition: Patient with non-resectable liver metastases from cholangiocarcinoma. A phase II trial. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2017-004444-38 | Sponsor Protocol Number: GAIN/GEM/CIS | Start Date*: 2019-01-11 | ||||||||||||||||||||||||||||||||||||
Sponsor Name:Krankenhaus Nordwest gGmbH | ||||||||||||||||||||||||||||||||||||||
Full Title: Neoadjuvant chemotherapy with gemcitabine plus cisplatin followed by radical liver resection versus immediate radical liver resection alone with or without adjuvant chemotherapy in incidentally det... | ||||||||||||||||||||||||||||||||||||||
Medical condition: incidental gallbladder carcinoma (IGBC) or biliary tract cancer (BTC) (intrahepatic cholangiocarcinoma (ICC)/ extrahepatic cholangiocarcinoma (ECC)) | ||||||||||||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||||||||||||
Trial protocol: DE (Completed) AT (Prematurely Ended) | ||||||||||||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2013-001688-22 | Sponsor Protocol Number: 01CCRe-IV | Start Date*: 2013-08-23 | |||||||||||
Sponsor Name:Servicio de Cirugía General y Digestiva Hospital Universitario de Bellvitge | |||||||||||||
Full Title: Randomized multicenter trial in colorectal cancer patients with non-resectable metastasis. Impact of tumor resection versus chemotherapy alone in survival. | |||||||||||||
Medical condition: Cancer colorectal stage IV with synchronous non-resectable metastasis. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2004-000327-15 | Sponsor Protocol Number: XL119-001 | Start Date*: 2004-11-25 | |||||||||||
Sponsor Name:Exelixis, Inc. | |||||||||||||
Full Title: A Phase 3 Multicenter, Single-Blind, Randomized Study of XL119 Versus 5-Fluorouracil (5-FU) plus Leucovorin (LV) in Subjects with Advanced Bilary Tumors Not Amenable to Coventional Surgery | |||||||||||||
Medical condition: Advanced Bilary Tract Tumours: Gall bladder cancer and Cholangiocarcinoma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) GB (Prematurely Ended) BE (Completed) IT (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2021-002629-95 | Sponsor Protocol Number: 170188 | Start Date*: 2022-08-02 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Sponsor Name:Department of vascular surgery, Lillebaelt Hospital | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Full Title: Cefuroxime and Piperacillin Concentrations in the Biliary System | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Medical condition: Infection in the biliary system such as cholecystitis and cholangitis both as acute infections and post-operative infections. | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Trial protocol: DK (Completed) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2014-003174-17 | Sponsor Protocol Number: GA1405 | Start Date*: 2015-03-24 |
Sponsor Name:Reckitt Benckiser Healthcare (UK) Limited | ||
Full Title: A multicentre, randomised, double-blind, two arm, parallel group, placebo controlled pivotal study to assess the effect of a sodium alginate liquid suspension as add-on therapy in GORD patients wit... | ||
Medical condition: Gastro-Oesophageal Reflux Disease (GORD) | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2018-002936-26 | Sponsor Protocol Number: 17-157 | Start Date*: 2019-11-28 |
Sponsor Name:Heinrich-Heine-University Düsseldorf | ||
Full Title: Efficacy and safety of Trifluridine/Tipiracil in combination with Irinotecan as a second line therapy in patients with Cholangiocarcinoma | ||
Medical condition: Patients with advanced, non resectable or metastatic cholangio- and gallbladder carcinoma after failure to respond to a previous gemcitabine treatment. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2016-003709-33 | Sponsor Protocol Number: AIO-HEP-0116 | Start Date*: 2017-05-04 | |||||||||||||||||||||||||||||||
Sponsor Name:AIO-Studien-gGmbH | |||||||||||||||||||||||||||||||||
Full Title: A randomized phase II trial of nal-IRI and 5-Fluorouracil compared to 5-Fluorouracil in patients with cholangio- and gallbladder carcinoma previously treated with gemcitabine-based therapies | |||||||||||||||||||||||||||||||||
Medical condition: advanced, unresectable and metastatic cholangio- and gallbladder carcinoma | |||||||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||||||||||||
Trial protocol: DE (Completed) | |||||||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2005-004636-52 | Sponsor Protocol Number: 2005AN005 | Start Date*: 2006-02-20 |
Sponsor Name:Heart of England NHS Foundation Trust | ||
Full Title: Randomised Double-Blind Placebo Controlled Trial of 40mg/day of Atorvastatin on Reduction in Severity of Sepsis in Ward Patients | ||
Medical condition: Sepsis is the clinical syndrome defined by the presence of both infection and a systemic inflammatory response. Sepsis is common in general medical and surgical wards with an estimated prevalence ... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (GB - no longer in EU/EEA) | ||
Trial results: (No results available) |
EudraCT Number: 2008-003327-23 | Sponsor Protocol Number: IP107-001 | Start Date*: 2008-10-29 | |||||||||||
Sponsor Name:Endo Pharmaceuticals Solutions Inc | |||||||||||||
Full Title: PHASE III, OPEN-LABEL, MULTICENTER INTERNATIONAL STUDY TO EVALUATE THE EFFICACY AND SAFETY OF AN OCTREOTIDE IMPLANT VERSUS SANDOSTATIN LAR® DEPOT IN PATIENTS WITH ACROMEGALY | |||||||||||||
Medical condition: Acromegaly | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: HU (Completed) CZ (Completed) PL (Completed) DE (Completed) ES (Completed) SK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2020-003359-13 | Sponsor Protocol Number: 21136 | Start Date*: 2020-12-16 | |||||||||||||||||||||
Sponsor Name:Bayer AG | |||||||||||||||||||||||
Full Title: A Multi-indication, Single-treatment Arm, Open-label Phase 2 Study of Regorafenib and Nivolumab in Combination with dose in Patients with Recurrent or Metastatic Solid Tumors | |||||||||||||||||||||||
Medical condition: Solid Tumors | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) FR (Completed) BE (Completed) IT (Completed) | |||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2014-003656-31 | Sponsor Protocol Number: UCL/14/0174 | Start Date*: 2015-07-31 | ||||||||||||||||
Sponsor Name:University College London | ||||||||||||||||||
Full Title: Addition of stereotactic body radiotherapy to systemic chemotherapy in locally advanced biliary tract cancers | ||||||||||||||||||
Medical condition: Locally advanced biliary tract cancer | ||||||||||||||||||
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Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2015-002066-24 | Sponsor Protocol Number: PrE0204 | Start Date*: 2015-08-28 |
Sponsor Name:The All Ireland Cooperative Oncology Research Group (ICORG) | ||
Full Title: A Multi-Institutional, Single Arm, Two-Stage Phase II Trial of Nab-Paclitaxel and Gemcitabine for First-Line Treatment of Patients with Advanced or Metastatic Cholangiocarcinoma | ||
Medical condition: Advanced or metastatic cholangiocarcinoma | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: AT (Completed) | ||
Trial results: View results |
EudraCT Number: 2019-003317-33 | Sponsor Protocol Number: CyPep-1 | Start Date*: 2019-12-31 |
Sponsor Name:Cytovation ASA | ||
Full Title: A first-in-human, open-label, dose escalation followed by dose expansion phase I/IIa trial to evaluate the safety, preliminary efficacy and pharmacokinetics of intratumoral CyPep-1 monotherapy and ... | ||
Medical condition: Histologically or cytologically confirmed locally advanced (unresectable) or metastatic tumors (solid tumors or lymphoma) with an accessible tumor lesion for intratumoral injection of CyPep-1 that ... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Completed) FR (Completed) ES (Ongoing) | ||
Trial results: View results |
EudraCT Number: 2009-015864-32 | Sponsor Protocol Number: DORIPED3001 | Start Date*: 2010-05-28 | |||||||||||
Sponsor Name:Janssen-Cilag International NV, Turnhoutseweg 30, 2340 Beerse, Belgium | |||||||||||||
Full Title: A Prospective, Randomized, Double-Blind, Multicenter Study to Establish the Safety and Tolerability of Doripenem Compared With Meropenem in Hospitalized Children With Complicated Intra-Abdominal In... | |||||||||||||
Medical condition: Complicated Intra-Abdominal Infections | |||||||||||||
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Population Age: Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: LT (Prematurely Ended) LV (Prematurely Ended) Outside EU/EEA | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-003572-23 | Sponsor Protocol Number: GCP#01.01.030 | Start Date*: 2017-12-27 | ||||||||||||||||
Sponsor Name:Gamida Cell Ltd | ||||||||||||||||||
Full Title: Allogeneic Stem Cell Transplantation of CordIn™, Umbilical Cord Blood-Derived Ex Vivo Expanded Stem and Progenitor Cells, in Patients with Hemoglobinopathies | ||||||||||||||||||
Medical condition: Hemoglobinopathies | ||||||||||||||||||
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Population Age: Children, Adolescents, Under 18, Adults | Gender: Male, Female | |||||||||||||||||
Trial protocol: FR (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2018-003747-37 | Sponsor Protocol Number: MK-7902-005 | Start Date*: 2019-03-07 | |||||||||||
Sponsor Name:Merck Sharp & Dohme Corp., a subsidiary of Merck & Co., Inc. | |||||||||||||
Full Title: A Multicenter, Open-label Phase 2 Study of Lenvatinib (E7080/MK-7902) Plus Pembrolizumab (MK-3475) in Previously Treated Subjects with Selected Solid Tumors (LEAP-005) | |||||||||||||
Medical condition: Triple negative breast cancer (TNBC), ovarian cancer, gastric cancer, colorectal cancer (CRC), glioblastoma (GBM), or biliary tract cancers (BTC) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) DE (Completed) GB (GB - no longer in EU/EEA) IT (Completed) | |||||||||||||
Trial results: (No results available) |
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