At a glance
ClinicalIndex Comparison RecordPhase 2Completed· 50 enrolled
Drug / intervention
Gemcitabine +2 moredrug
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.
Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.
A Feasibility Phase II Study of Gemcitabine With Docetaxel With Concurrent 3-D Conformal Radiation Plus Continuous Infusion 5-Fluorouracil in the Treatment of Resected Cholangiocarcinoma, Gallbladder, Pancreatic and Ampullary Cancers
In Brief
A Phase 2 clinical trial evaluating Gemcitabine, Docetaxel, and 1 other intervention for Cholangiocarcinoma Cancer and 3 related conditions. Completed, enrolled 50 participants across 1 site.
Detailed Summary
To assess the feasibility of administering induction chemotherapy with gemcitabine and docetaxel followed by concurrent radiation and continuous infusion 5FU and consolidation gemcitabine/docetaxel chemotherapy.
Study Details
Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesUnited States
Collaborators--
Timeline
Phase 2CompletedFinished
20022003200420052006200720082009201020112012201320142015201620172018201920202021202220232024202520262027
Enrollment StartSep 2002
First PostedApr 2008
Primary CompletionSep 2010
Study CompletionSep 2012
TodayJul 2026
First PostedApr 17, 2008
Enrollment StartSep 1, 2002
Primary CompletionSep 1, 2010
Study CompletionSep 1, 2012
TodayJul 2, 2026
Enrollment to primary: 8 yearsPosted 18.2 years ago
Interventions
Gemcitabinedrug
Docetaxeldrug
Radiationradiation