TerminatedPhase 2NCT04099888
PCI Treatment/Gemcitabine & Chemotherapy vs Chemotherapy Alone in Patients With Inoperable Extrahepatic Bile Duct Cancer
Studying Perihilar cholangiocarcinoma
Last synced from ClinicalTrials.gov
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Clinical trial records are synced from ClinicalTrials.gov through automated extraction.
Report missing dataKey facts
- Sponsor
- PCI Biotech AS
- Principal Investigator
- PCI BiotechPCI Biotech
- Intervention
- Fimaporfin and Gemcitabine(drug)
- Enrollment
- 41 enrolled
- Eligibility
- 18 years · All sexes
- Timeline
- 2019 – 2022
Study locations (30)
- City of Hope National Medical Center, Duarte, California, United States
- Emory University Hospital, 1365C Clifton Road NE, Atlanta, Georgia, United States
- University of Chicago Medical Center, 5841 South Maryland Avenue, Chicago, Illinois, United States
- University of Louisville, Louisville, Kentucky, United States
- The Mayo Clinic Hospital - Saint Mary's Campus, 1216 Second Street Southwest, Rochester, Minnesota, United States
- Baylor College of Medicine, Houston, Texas, United States
- UZ Gent, Ghent, Oost-Vlaanderen, Belgium
- UZ Leuven, Leuven, Belgium
- Odense Universitetshospital, Odense, Denmark
- Tampereen yliopistollinen sairaala, Syöpätautien klinikka, Tampere, Finland
- Centre Hospitalier Universitaire Grenoble Alpes - Hopital Albert Michallon, Grenoble, Cedex 09, France
- CHU Angers, Angers, Cedex 9, France
- CHU Dupuytren, 2 Avenue Martin Luther King, Limoges, France
- Institut Gustave Roussy, Département de gastro-entérologie, Villejuif, France
- Klinikum rechts der Isar der Technischen Universität München, München, Bavaria, Germany
- +15 more locations on ClinicalTrials.gov
Primary source
Recruitment status, site addresses, contacts, and full eligibility criteria can change between syncs. Always verify with the trial team before planning travel or treatment.
Open NCT04099888 on ClinicalTrials.govOther trials for Perihilar cholangiocarcinoma
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