CI

At a glance

ClinicalIndex Comparison Record
Phase 2Completed· 32 enrolled
Drug / intervention
Bevacizumab +2 moredrug
Likely dose
Gemcitabine intravenously days 1, 8, 15 of 28-day cycle; Bevacizumab intravenously days 1 and 25 of 28-day cycle; Erlotinib orally dailyAI-extracted
Key inclusion· 8
  • Previously untreated unresectable or metastatic pancreatic adenocarcinoma
  • ECOG Performance Status 0-2
  • Age 18 years or older
  • Radiographically measurable disease
Key exclusion· 12
  • Prior treatment with tyrosine kinase inhibitor, EGFR inhibitor, or VEGF inhibitor
  • Warfarin anticoagulation
  • CNS or brain metastases
  • Blood pressure >150/100 mmHg

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT00366457
NCT00366457Phase 2Completed

Phase II Study of Gemcitabine, Bevacizumab and Erlotinib in Locally Advanced and Metastatic Pancreatic Cancer

Massachusetts General Hospital·interventional·Posted Aug 21, 2006·Updated May 15, 2017

In Brief

A Phase 2 clinical trial evaluating Bevacizumab, Erlotinib, and 1 other intervention for Pancreatic Cancer and Adenocarcinoma of the Pancreas. Completed, enrolled 32 participants across 3 sites.

Detailed Summary

The main purpose of this study is to learn whether or not the combination of gemcitabine, bevacizumab and erlotinib works in treating patients with advanced or metastatic pancreatic cancer. Bevacizumab is a new anti-cancer drug. It is an antibody that works to slow or stop cell growth in cancerous tumors by decreasing the blood supply to the tumors. It is approved by the FDA for the treatment of colorectal cancer but is still considered investigational for treating pancreatic cancer.

Study Details

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

Timeline

Phase 2CompletedFinished
200720082009201020112012201320142015201620172018201920202021202220232024202520262027
First PostedAug 21, 2006
Enrollment StartAug 1, 2006
Primary CompletionAug 1, 2008
Study CompletionJul 1, 2011
TodayJul 2, 2026
Enrollment to primary: 2 yearsPosted 19.9 years ago

Interventions

Bevacizumabdrug

Given intravenously on days 1 and 25 of every 28-day cycle (one every 2 weeks). Participants may continue to receive study treatment as long as there is no disease progression or serious side effects.

Erlotinibdrug

Taken orally every day. Participants may continue to receive study treatment as long as there is no disease progression or serious side effects.

Gemcitabinedrug

Given intravenously on days 1, 8 and 15 of each 28-day cycle. Participants may continue to receive study treatment as long as there is no disease progression or serious side effects.