- Trials with a EudraCT protocol (127)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (3)
127 result(s) found for: cholangiocarcinoma.
Displaying page 1 of 7.
EudraCT Number: 2013-004854-46 | Sponsor Protocol Number: 1333 | Start Date*: 2014-04-04 | |||||||||||
Sponsor Name:Herlev University Hospital | |||||||||||||
Full Title: Randomized 1. Line treatment with gemcitabine, capecitabine, oxaliplatin vs gemcitabin and cisplatin to patients with cholangiocarcinoma. | |||||||||||||
Medical condition: patient with metastatic cholangiocarcinoma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-001559-11 | Sponsor Protocol Number: 1312 | Start Date*: 2013-09-13 | |||||||||||
Sponsor Name:Herlev University Hospital | |||||||||||||
Full Title: Chemotherapy with gemcitabine, capecitabine, irinotecan and bevacizumab to patients with cholangiocarcinoma after progression on first line treatment. | |||||||||||||
Medical condition: patients with cholangiocarcinoma after progression. When patients with cholangiocarcinoma cannot be operated, we cannot cure them. The purpose of oncologic treatment is to prolong survival and to e... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2004-003990-10 | Sponsor Protocol Number: PHOCCC04-01 | Start Date*: 2005-01-18 | |||||||||||
Sponsor Name:Axcan Pharma Inc. (Axcan Pharma International B.V. is a subsidiary of Axcan Pharma Inc.) | |||||||||||||
Full Title: Multicenter, open-label, randomised, controlled phase III clinical study of the efficacy and safety of photodynamic therapy using porfimer sodium for injection as palliative treatment for unresecta... | |||||||||||||
Medical condition: Unresectable Cholangiocarcinoma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-001560-37 | Sponsor Protocol Number: GEM-658-EBE-0024-I | Start Date*: Information not available in EudraCT | |||||||||||
Sponsor Name:Medizinische Fakultät der TU-München, vertreten durch den Dekan | |||||||||||||
Full Title: Sequentielle Kombination einer Chemotherapie mit Gemcitabine/Oxaliplatin und photodynamischen Therapie beim fortgeschrittenen Gallengangskarzinom | |||||||||||||
Medical condition: - advanced cholangiocarcinoma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-011897-14 | Sponsor Protocol Number: CLIN904 CCM201 | Start Date*: 2009-07-08 | |||||||||||
Sponsor Name:STEBA BIOTECH | |||||||||||||
Full Title: EVALUATION OF THE SAFETY AND EFFICACY OF WST11-MEDIATED VASCULAR TARGETED PHOTODYNAMIC THERAPY ON NON-RESECTABLE OR INOPERABLE CHOLANGIOCARCINOMA | |||||||||||||
Medical condition: Non-resectable or inoperable cholangiocarcinoma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2018-002894-23 | Sponsor Protocol Number: INCB54828-302 | Start Date*: 2019-05-30 | |||||||||||
Sponsor Name:Incyte Corporation | |||||||||||||
Full Title: A Phase 3, Open-Label, Randomized, Active-Controlled, Multicenter Study to Evaluate the Efficacy and Safety of Pemigatinib Versus Gemcitabine Plus Cisplatin Chemotherapy in First-Line Treatment of ... | |||||||||||||
Medical condition: Male and female participants at least 18 years of age who have unresectable and/or metastatic cholangiocarcinoma with FGFR2 rearrangement | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) SE (Trial now transitioned) DE (Trial now transitioned) AT (Trial now transitioned) FI (Completed) FR (Trial now transitioned) BE (Trial now transitioned) NO (Completed) NL (Trial now transitioned) ES (Ongoing) DK (Completed) IT (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2016-002422-36 | Sponsor Protocol Number: INCB54828-202 | Start Date*: 2017-05-04 | |||||||||||
Sponsor Name:Incyte Corporation | |||||||||||||
Full Title: A Phase 2, Open-Label, Single-Arm, Multicenter Study to Evaluate the Efficacy and Safety of INCB054828 in Subjects With Advanced/Metastatic or Surgically Unresectable Cholangiocarcinoma Including F... | |||||||||||||
Medical condition: Subjects with advanced/metastatic or surgically unresectable cholangiocarcinoma with FGFR2 translocations, with other FGF/FGFR alterations, or who are negative for any FGF/FGFR alterations, who fai... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) BE (Completed) FR (Completed) GB (GB - no longer in EU/EEA) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2022-003787-24 | Sponsor Protocol Number: PM-CARE-PNRR-MAD-2022-12375905 | Start Date*: 2023-04-20 | ||||||||||||||||
Sponsor Name:OSPEDALE SAN RAFFAELE | ||||||||||||||||||
Full Title: Precision Medicine in patients with unresectable CholAngiocarcinoma; RadioEmbolization and combined biological therapy (Single arm, multicenter phase II study investigating the efficacy and safety... | ||||||||||||||||||
Medical condition: Unresectable intrahepatic cholangiocarcinoma | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: IT (Trial now transitioned) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2013-005085-19 | Sponsor Protocol Number: CBGJ398X2204 | Start Date*: 2014-06-30 | |||||||||||
Sponsor Name:Novartis Farmacéutica, S.A. | |||||||||||||
Full Title: A phase II multicenter, single arm study of oral BGJ398 in adult patients with advanced or metastatic cholangiocarcinoma with FGFR2 gene fusions or other FGFR genetic alterations who failed or are ... | |||||||||||||
Medical condition: advanced or metastatic cholangiocarcinoma FGFR2 gene fusion, FGFR genetic alteration | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) BE (Completed) IT (Completed) DE (Completed) GB (GB - no longer in EU/EEA) | |||||||||||||
Trial results: View results |
EudraCT Number: 2004-001126-24 | Sponsor Protocol Number: AGO/GAS/04/01 | Start Date*: 2004-10-25 |
Sponsor Name:University Hospital Ghent | ||
Full Title: Feasibility of radiotherapy and concomitant gemcitabine and oxaliplatin in locally advanced pancreatic cancer and distal cholangiocarcinoma | ||
Medical condition: Pancreatic cancer or distal cholangiocarcinoma | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: BE (Completed) | ||
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: 2020-004938-38 | Sponsor Protocol Number: ADVANCE2020 | Start Date*: 2021-12-08 | ||||||||||||||||||||||||||
Sponsor Name:Frankfurter Institut für Klinische Krebsforschung IKF GmbH | ||||||||||||||||||||||||||||
Full Title: ADVANCE: A phase II single-arm, open-label study of Atezolizumab and Derazantinib for patients with advanced intrahepatic cholangiocarcinoma with FGFR2 fusions/rearrangements | ||||||||||||||||||||||||||||
Medical condition: Advanced non-resectable intrahepatic cholangiocarcinoma with positively confirmed FGFR2 fusion/rearrangements via NGS-Analysis | ||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: DE (Trial now transitioned) | ||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2023-000138-13 | Sponsor Protocol Number: CITATION | Start Date*: 2023-04-05 | |||||||||||
Sponsor Name:ISTITUTO NAZIONALE TUMORI - IRCCS FONDAZIONE PASCALE | |||||||||||||
Full Title: Neo-adjuvant Chemo and immunotherapy with durvalumab (MEDI4736) and tremelimumab (MEDI1123) In The pre-operAtive Treatment of locally advanced cholangIOcarciNoma: an exploratory and translational s... | |||||||||||||
Medical condition: Locally advanced cholangiocarcinoma patients | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2010-020385-13 | Sponsor Protocol Number: 52702928 | Start Date*: 2010-06-21 | |||||||||||
Sponsor Name:Vejle Hospital | |||||||||||||
Full Title: Randomized phase II trial of combination chemotherapy with panitumumab or bevacizumab for patients with inoperable cholangiocarcinoma without KRAS mutations | |||||||||||||
Medical condition: Inoperable cholangiocarcinoma without KRAS mutations | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) SE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2015-005117-72 | Sponsor Protocol Number: AG120-C-005 | Start Date*: 2017-04-24 | ||||||||||||||||
Sponsor Name:Agios Pharmaceuticals, Inc. | ||||||||||||||||||
Full Title: A Phase 3, Multicenter, Randomized, Double-Blind, Placebo-controlled Study of AG-120 in Previously-treated Subjects with Nonresectable or Metastatic Cholangiocarcinoma with an IDH1 Mutation | ||||||||||||||||||
Medical condition: Nonresectable or Metastatic Cholangiocarcinoma | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: DE (Completed) GB (GB - no longer in EU/EEA) ES (Completed) FR (Completed) IT (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2018-002647-29 | Sponsor Protocol Number: PCIA_203/18 | Start Date*: 2019-03-27 | |||||||||||
Sponsor Name:PCI Biotech AS | |||||||||||||
Full Title: A Multi-Centre, Randomised, Open-Label, Phase 2 Study to Assess the Safety, Tolerability and Efficacy of Fimaporfin-Induced Photochemical Internalisation of Gemcitabine Complemented by Gemcitabine/... | |||||||||||||
Medical condition: Inoperable Cholangiocarcinoma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) NO (Completed) SE (Completed) ES (Prematurely Ended) DK (Completed) FI (Completed) BE (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-002367-14 | Sponsor Protocol Number: 39672894 | Start Date*: 2008-06-27 | |||||||||||
Sponsor Name:Vejle Sygehus | |||||||||||||
Full Title: Kombineret biologisk behandling og kemoterapi til patienter med inoperabelt cholangiocarcinom | |||||||||||||
Medical condition: Inoperabelt cholangiocarcinom | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) SE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-005850-22 | Sponsor Protocol Number: 62202-788 | Start Date*: 2008-07-28 | |||||||||||
Sponsor Name:BGDO | |||||||||||||
Full Title: GEMCITABINE AND CETUXIMAB IN PATIENTS WITH ADVANCED OR METASTATIC BILIARY TRACT CANCER: A BGDO MULTICENTER PHASE II STUDY | |||||||||||||
Medical condition: Patients with advanced biliary tract cancer, excluding gallbladder cancer, where surgery is not feasible. | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-001705-24 | Sponsor Protocol Number: HE37/12 | Start Date*: 2013-02-20 | |||||||||||||||||||||
Sponsor Name:Hellenic Cooperative Oncology Group | |||||||||||||||||||||||
Full Title: Phase II single-arm study of first line treatment with gemcitabine and pazopanib in patients with inoperable locally advanced or metastatic biliary tree cancer (cholangiocarcinoma or gallbladder ca... | |||||||||||||||||||||||
Medical condition: Inoperable locally advanced or metastatic cancer of the biliary tree (cholangiocarcinoma and gallbladder carcinoma) | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: GR (Prematurely Ended) | |||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2010-018850-11 | Sponsor Protocol Number: MHH_CCA_AG54 | Start Date*: 2011-04-15 | ||||||||||||||||
Sponsor Name:Medizinische Hochschule Hannover (MHH) | ||||||||||||||||||
Full Title: Panitumumab in combination with cisplatin/gemcitabine chemotherapy in patients with cholangiocarcinomas - a randomized clinical phase II study - PiCCA Study | ||||||||||||||||||
Medical condition: cholangiocarcinoma / gall bladder carcinoma | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Female | |||||||||||||||||
Trial protocol: DE (Completed) | ||||||||||||||||||
Trial results: View results |
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