- 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 3 of 7.
EudraCT Number: 2015-001443-36 | Sponsor Protocol Number: ARQ087-101 | Start Date*: 2015-08-05 | ||||||||||||||||
Sponsor Name:ARQULE INC | ||||||||||||||||||
Full Title: A Phase 1/2 Study of ARQ 087 in Adult Subjects with Advanced Solid Tumors with FGFR Genetic Alterations, Including Intrahepatic Cholangiocarcinoma with FGFR2 Gene Fusion | ||||||||||||||||||
Medical condition: Advanced Solid Tumors with FGFR Genetic Alterations, Including Intrahepatic Cholangiocarcinoma with FGFR2 Gene Fusion | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: IT (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2018-000257-45 | Sponsor Protocol Number: MO40094 | Start Date*: 2021-07-19 | |||||||||||
Sponsor Name:University Hospital Essen | |||||||||||||
Full Title: A phase Ib/II single-arm study evaluating the safety and efficacy of combined immunotherapy with mFOLFOX6, bevacizumab and atezolizumab in advanced-stage biliary cancer | |||||||||||||
Medical condition: advanced biliary tract cancer (BTC) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2021-002389-41 | Sponsor Protocol Number: ADJUBIL | Start Date*: 2022-02-25 | |||||||||||||||||||||||||||||||||||||||||
Sponsor Name:Frankfurter Institut für Klinische Krebsforschung IKF GmbH am Krankenhaus Nordwest | |||||||||||||||||||||||||||||||||||||||||||
Full Title: A Phase II study of immunotherapy with durvalumab and tremelimumab in combination with capecitabine or without capecitabine in adjuvant situation for biliary tract cancer | |||||||||||||||||||||||||||||||||||||||||||
Medical condition: biliary tract cancer | |||||||||||||||||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||||||||||||||||||||||
Trial protocol: DE (Trial now transitioned) | |||||||||||||||||||||||||||||||||||||||||||
Trial results: (No results available) |
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: 2021-004411-11 | Sponsor Protocol Number: NeoTreme | Start Date*: 2023-05-03 | |||||||||||
Sponsor Name: University Hospital Schleswig-Holstein, Campus Lübeck | |||||||||||||
Full Title: Phase 2 Study of Preoperative Gemcitabine Plus Cisplatin with Durvalumab (MEDI4736) and Tremelimumab in intrahepatic cholangiocarcinoma (NeoTreme) | |||||||||||||
Medical condition: Intrahepatic cholangiocarcinoma | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2021-005605-27 | Sponsor Protocol Number: TNG908-C101 | Start Date*: 2022-09-07 | ||||||||||||||||||||||||||||||||||||||||||||||
Sponsor Name:Tango Therapeutics, Inc. | ||||||||||||||||||||||||||||||||||||||||||||||||
Full Title: A Phase 1/2, Multi-Center, Open-Label Study to Evaluate the Safety, Tolerability, and Preliminary Anti-tumor Activity of TNG908 in Patients with MTAP-deleted Advanced or Metastatic Solid Tumors | ||||||||||||||||||||||||||||||||||||||||||||||||
Medical condition: Phase 1: • Locally advanced or metastatic MTAP-deleted solid tumors (with the exception of gliomas) Phase 2: • Arm 1: Locally advanced or metastatic MTAP-deleted squamous and nonsquamous NSCLC ... | ||||||||||||||||||||||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||||||||||||||||||||||
Trial protocol: FR (Trial now transitioned) | ||||||||||||||||||||||||||||||||||||||||||||||||
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: 2016-004448-12 | Sponsor Protocol Number: ARQ087-301 | Start Date*: 2017-12-18 | ||||||||||||||||
Sponsor Name:ARQULE INC | ||||||||||||||||||
Full Title: A Pivotal Trial of ARQ 087 in Subjects with FGFR2 Gene Fusion Positive Inoperable or Advanced Intrahepatic Cholangiocarcinoma | ||||||||||||||||||
Medical condition: Inoperable or advanced FGFR2 gene fusion positive intrahepatic cholangiocarcinoma | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: IT (Completed) GB (GB - no longer in EU/EEA) DE (Completed) IE (Completed) ES (Ongoing) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2017-000123-28 | Sponsor Protocol Number: IJB-MULTI-MIME-A-2017 | Start Date*: 2018-11-14 | |||||||||||||||||||||||||||||||
Sponsor Name:Institut Jules Bordet | |||||||||||||||||||||||||||||||||
Full Title: Multiorgan Metabolic imaging response assessment of Abemaciclib: the MiMe-A trial | |||||||||||||||||||||||||||||||||
Medical condition: esophageal ADC, esophageal SCC, Cholangiocarcinoma, urothelial cancer (progressive after immunotherapy), or endometrial cancer | |||||||||||||||||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||||||||||||||||||||||
Trial protocol: BE (Completed) FR (Completed) | |||||||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2019-004217-14 | Sponsor Protocol Number: P21.128 | Start Date*: 2022-11-09 |
Sponsor Name:Leiden University Medical Center | ||
Full Title: FLUOPANC-trial - Intraoperative near-infrared fluorescence imaging in pancreatic- and extrahepatic bile duct tumors using cRGD-ZW800-1 and dedicated imaging systems: A phase II feasibility, dose-ra... | ||
Medical condition: Pancreatic cancer (pancreatic carcinoma) Extrahepatic bile duct cancer (cholangiocarcinoma) | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2018-004778-81 | Sponsor Protocol Number: IMMUWHY | Start Date*: 2019-10-29 | ||||||||||||||||
Sponsor Name:Institut für Klinische Krebsforschung IKF GmbH | ||||||||||||||||||
Full Title: A phase II study of immunotherapy with durvalumab (MEDI4736) or durvalumab and tremelimumab, both combined with Y-90 SIRT therapy in patients with advanced stage intrahepatic biliary tract cancer (... | ||||||||||||||||||
Medical condition: Intrahepatic Biliary Tract Carcinoma | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: DE (Trial now transitioned) | ||||||||||||||||||
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: 2022-003217-11 | Sponsor Protocol Number: NL82304.058.22 | Start Date*: 2023-02-24 | |||||||||||||||||||||
Sponsor Name:Leiden University Medical Center | |||||||||||||||||||||||
Full Title: Standard versus Pre-emptive Antibiotic Treatment to Reduce the Rate of Infectious Outcomes after Whipple procedure (SPARROW): a multicenter, randomized controlled trial | |||||||||||||||||||||||
Medical condition: Pancreatic head malignancy | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: NL (Trial now transitioned) | |||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2022-001843-25 | Sponsor Protocol Number: BNT141-01 | Start Date*: 2023-02-23 | ||||||||||||||||||||||||||||||||||||||||||||||
Sponsor Name:BioNTech SE | ||||||||||||||||||||||||||||||||||||||||||||||||
Full Title: Phase I/IIa, first-in-human, open-label, dose escalation trial with expansion cohorts to evaluate safety, pharmacokinetics, pharmacodynamics, and preliminary efficacy of BNT141 as a monotherapy and... | ||||||||||||||||||||||||||||||||||||||||||||||||
Medical condition: CLDN18.2-positive solid tumors | ||||||||||||||||||||||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||||||||||||||||||||||
Trial protocol: DK (Prematurely Ended) ES (Prematurely Ended) NL (Ongoing) | ||||||||||||||||||||||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2013-004810-16 | Sponsor Protocol Number: TPU-TAS-120-101 | Start Date*: 2014-04-10 | |||||||||||
Sponsor Name:Taiho Oncology Inc | |||||||||||||
Full Title: PHASE 1/2 STUDY OF TAS-120 IN PATIENTS WITH ADVANCED SOLID TUMORS HARBORING FGF/FGFR ABERRATIONS | |||||||||||||
Medical condition: Advanced solid tumors | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) ES (Completed) DE (Completed) NL (Completed) PT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2019-002113-19 | Sponsor Protocol Number: 42756493CAN2002 | Start Date*: 2019-10-31 | |||||||||||
Sponsor Name:Janssen-Cilag International NV | |||||||||||||
Full Title: A Phase 2 Study of Erdafitinib in Subjects with Advanced Solid Tumors and FGFR Gene Alterations | |||||||||||||
Medical condition: Advanced solid tumors (other than Urothelial tumors), and FGFR gene alterations. | |||||||||||||
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Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) PL (Completed) FR (Completed) DE (Trial now transitioned) ES (Ongoing) BE (Completed) IT (Completed) Outside EU/EEA SE (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2021-006386-38 | Sponsor Protocol Number: 20210104 | Start Date*: 2022-06-02 | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Sponsor Name:Amgen, Inc. | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Full Title: A Phase 1b/2, Multicenter, Open-label Basket Study Evaluating the Safety and Efficacy of Bemarituzumab Monotherapy in Solid Tumors with FGFR2b Overexpression (FORTITUDE 301) | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Medical condition: A Phase 1b/2, Multicenter, Open-label Basket Study Evaluating the Safety and Efficacy of Bemarituzumab Monotherapy in Solid Tumors with FGFR2b Overexpression | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Trial protocol: CZ (Trial now transitioned) FR (Trial now transitioned) ES (Temporarily Halted) AT (Trial now transitioned) IT (Trial now transitioned) HU (Trial now transitioned) BE (Trial now transitioned) NL (Trial now transitioned) PT (Trial now transitioned) DK (Trial now transitioned) FI (Trial now transitioned) BG (Trial now transitioned) RO (Trial now transitioned) | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2019-004630-42 | Sponsor Protocol Number: TAS-120-301 | Start Date*: 2021-01-25 | |||||||||||
Sponsor Name:Taiho Oncology Inc | |||||||||||||
Full Title: A Phase 3, Open-Label, Randomized Study of Futibatinib Versus Gemcitabine-Cisplatin Chemotherapy as First-Line Treatment of Patients with Advanced Cholangiocarcinoma Harboring FGFR2 Gene Rearrangem... | |||||||||||||
Medical condition: Advanced solid tumors | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) PT (Prematurely Ended) DE (Prematurely Ended) PL (Completed) IT (Prematurely Ended) | |||||||||||||
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: 2009-013408-30 | Sponsor Protocol Number: 2009-013408-30 | Start Date*: 2010-08-23 | |||||||||||||||||||||
Sponsor Name:University College London | |||||||||||||||||||||||
Full Title: Randomised phase II trial of cediranib (AZD2171) vs. placebo in addition to cisplatin / gemcitabine chemotherapy for patients with advanced biliary tract cancers | |||||||||||||||||||||||
Medical condition: biliary tract carcinomas (including gallbladder cancer and cholangiocarcinomas) | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: GB (Completed) | |||||||||||||||||||||||
Trial results: View results |
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