CI

At a glance

ClinicalIndex Comparison Record
Phase 2Completed· 39 enrolled
Drug / intervention
gemcitabine hydrochloride +7 moredrug
Likely dose
gemcitabine hydrochloride 1,000 mg/m2from 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.

Search/NCT00536874
NCT00536874Phase 2Completed

A Phase II Study of Neoadjuvant Gemcitabine and Oxaliplatin in Patients With Potentially Resectable Previously Untreated Pancreatic Adenocarcinoma

Memorial Sloan Kettering Cancer Center·interventional·Posted Sep 28, 2007·Updated Mar 16, 2017

In Brief

A Phase 2 clinical trial evaluating gemcitabine hydrochloride, oxaliplatin, and 6 other interventions for Pancreatic Cancer. Completed, enrolled 39 participants across 1 site.

Detailed Summary

RATIONALE: Drugs used in chemotherapy, such as gemcitabine and oxaliplatin, work in different ways to stop the growth of tumor cells, either by killing the cells or by stopping them from dividing. Giving chemotherapy before surgery may make the tumor smaller and reduce the amount of normal tissue that needs to be removed. Giving chemotherapy after surgery may kill any tumor cells that remain after surgery. PURPOSE: This phase II trial is studying how well giving gemcitabine together with oxaliplatin works in treating patients with pancreatic cancer that can be removed by surgery.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesUnited States

Timeline

Phase 2CompletedFinished
20082009201020112012201320142015201620172018201920202021202220232024202520262027
First PostedSep 28, 2007
Enrollment StartOct 1, 2007
Primary CompletionSep 1, 2012
Study CompletionFeb 1, 2017
TodayJul 2, 2026
Enrollment to primary: 4.9 yearsPosted 18.8 years ago

Interventions

gemcitabine hydrochloridedrug

1,000 mg/m2 IV over 100 minutes on day 1 every 14 days for 4 cycles

oxaliplatindrug

80 mg/m2 IV over 2 hours on day 1 every 14 days for 4 cycles.

protein expression analysisgenetic

proteomic profilinggenetic

diagnostic laboratory biomarker analysisother

adjuvant therapyprocedure

neoadjuvant therapyprocedure

therapeutic conventional surgeryprocedure