CI

At a glance

ClinicalIndex Comparison Record
Phase 2Completed· 45 enrolled
Drug / intervention
Gemcitabine +2 moredrug
Likely dose
Gemcitabine 1000 mgfrom 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/NCT00696696
NCT00696696Phase 2Completed

A Phase II Study of Gemcitabine and Erlotinib Plus Sorafenib (GES) in Metastatic Pancreatic Cancer

NYU Langone Health·interventional·Posted Jun 13, 2008·Updated Jun 30, 2016

In Brief

A Phase 2 clinical trial evaluating Gemcitabine, Erlotinib, and 1 other intervention for Pancreatic Cancer. Completed, enrolled 45 participants across 3 sites.

Detailed Summary

This study tests the combination of two targeted therapies,along with chemotherapy treatment in the treatment of pancreatic cancer.

Study Details

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

Timeline

Phase 2CompletedFinished
20082009201020112012201320142015201620172018201920202021202220232024202520262027
First PostedJun 13, 2008
Enrollment StartSep 1, 2007
Primary CompletionNov 1, 2010
Study CompletionJun 1, 2013
TodayJul 2, 2026
Enrollment to primary: 3.2 yearsPosted 18.1 years ago

Interventions

Gemcitabinedrug

1000 mg/m\^2, intravenous, Days 1, 8, 15 for every 28-day cycle. In the absence of disease progression or toxicity, a patient may continue to receive gemcitabine, erlotinib, and sorafenib until disease progression.

Erlotinibdrug

150 mg, taken orally, once a day, Days 1-28 for every 28-day cycle. In the absence of disease progression or toxicity, a patient may continue to receive gemcitabine, erlotinib, and sorafenib until disease progression.

Sorafenibdrug

400 mg, taken orally, twice a day, Days 1-28 for every 28-day cycle. In the absence of disease progression or toxicity, a patient may continue to receive gemcitabine, erlotinib, and sorafenib until disease progression.