CompletedPhase 1NCT01900158
A Phase I/II Safety and Efficacy Study of PCI of Gemcitabine and Chemotherapy in Patients With Cholangiocarcinomas
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
- Dr Richard Sturgess, MDUniversity Hospital Aintree
- Intervention
- Amphinex, Gemcitabine and Cisplatin(drug)
- Enrollment
- 24 enrolled
- Eligibility
- 18 years · All sexes
- Timeline
- 2013 – 2019
Study locations (11)
- CHU Angers, Angers, Maine-et-Loire, France
- Klinikum rechts der Isar, Technische Universität München, Munich, Bavaria, Germany
- Klinikum der Ludwig-Maximilians-Universität, München, Bavaria, Germany
- Klinikum der Johann Wolfgang Goethe-Universität, Frankfurt am Main, Hesse, Germany
- Universitätsklinikum Essen, Essen, North Rhine-Westphalia, Germany
- Klinikum Ludwigshafen, Ludwigshafen am Rhein, Rhineland-Palatinate, Germany
- Universitätsklinikum Leipzig, Leipzig, Saxony, Germany
- Charité, Campus Mitte, Berlin, Germany
- Universitätsklinikum Carl Gustav Carus an der Technischen Universität Dresden, Dresden, Germany
- Oslo Universtiy Hospital, Oslo, Norway
- University Hospital Aintree, Aintree, Liverpool, United Kingdom
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 NCT01900158 on ClinicalTrials.govOther trials for Perihilar cholangiocarcinoma
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