Clinical Trials Directory

Trials / Completed

CompletedNCT01058655

RAD001 and AV-951 in Patients With Refractory, Metastatic Colorectal Cancer

A Phase I/II Study of RAD001 and AV-951 in Patients With Refractory, Metastatic Colorectal Cancer

Status
Completed
Phase
Phase 1 / Phase 2
Study type
Interventional
Enrollment
56 (actual)
Sponsor
Dana-Farber Cancer Institute · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

Research has shown that anti-angiogenic agents can be effective therapies to treat cancer. Anti-angiogenic agents target the blood vessels required for tumors to grow. Vascular endothelial growth factor (VEGF) is one of the cell pathways used for this blood vessel growth. When the investigators interfere with the VEGF pathway, the investigators inhibit this blood vessel growth which is required by tumors. One of the study drugs being used, tivozanib (AV-951), selectively interferes with the VEGF pathway. The second study drug being used, everolimus (RAD001) interferes with the mTOR pathway. The mTOR pathway is another pathway involved in blood vessel and tumor cell growth. By combining these two drugs the investigators hope to slow or reverse tumor cell growth in patients whose tumors have become resistant to other therapies for their disease.

Detailed description

Primary Objective Phase I * To determine the safety, tolerability, and maximally tolerated dose (MTD) of everolimus and tivozanib administered in combination to patients with advanced gastrointestinal tumors. Phase II * At the MTD, to assess progression-free survival associated with everolimus and tivozanib in patients with refractory, metastatic colorectal cancer. Secondary Objectives Phase II * To assess tumor response rate. * To assess overall survival.

Conditions

Interventions

TypeNameDescription
DRUGEverolimus
DRUGTivozanib

Timeline

Start date
2010-02-01
Primary completion
2013-09-01
Completion
2015-04-01
First posted
2010-01-29
Last updated
2017-04-13
Results posted
2017-04-07

Locations

3 sites across 1 country: United States

Source: ClinicalTrials.gov record NCT01058655. Inclusion in this directory is not an endorsement.