CI

At a glance

ClinicalIndex Comparison Record
Phase 1Completed· 12 enrolled
Drug / intervention
CABOZANTINIB +1 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.

Search/NCT01663272
NCT01663272Phase 1Completed

A Trial of Cabozantinib (XL184) and Gemcitabine in Advanced Pancreatic Cancer

University of Michigan Rogel Cancer Center·interventional·Posted Aug 13, 2012·Updated Sep 19, 2018

In Brief

A Phase 1 clinical trial evaluating CABOZANTINIB and gemcitabine for Pancreatic Cancer. Completed, enrolled 12 participants across 1 site.

Detailed Summary

Gemcitabine is considered one of the standard drugs for advanced pancreatic cancer and is approved by the FDA to treat it. Cabozantinib is a new drug that has demonstrated effectiveness against pancreatic cancer in laboratory experiments, especially when given with gemcitabine. Initial studies with cabozantinib in pancreatic cancer have shown some activity against the disease. The purpose of this study is to determine the safest and highest dose of cabozantinib that can be given together with standard doses of gemcitabine in patients with pancreatic cancer. This study will determine the safety and tolerability of this two drug combination.

Study Details

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

Timeline

Phase 1CompletedFinished
20132014201520162017201820192020202120222023202420252026
First PostedAug 13, 2012
Enrollment StartJul 1, 2012
Primary CompletionJan 1, 2015
Study CompletionMar 1, 2017
TodayJul 2, 2026
Enrollment to primary: 2.5 yearsPosted 13.9 years ago

Interventions

CABOZANTINIBdrug

Daily oral cabozantinib administered days -7 until disease progression, intolerable adverse event(s) or patient choice.

gemcitabinedrug

Gemcitabine administered intravenously on days 1, 8, and 15 every 28 days.