Overview

Study in Locally Advanced Squamous Cell Carcinoma of Head and Neck

Status:
Terminated
Trial end date:
2015-01-01
Target enrollment:
Participant gender:
Summary
Primary Compare response rates (relative change in tumor size) to induction chemotherapy consisting of cisplatin/paclitaxel/cetuximab +/- everolimus. Secondary: Determine the maximum administered dose (MAD), maximum tolerated dose (MTD), dose limiting toxicity (DLT), and safety of everolimus with cisplatin/paclitaxel/cetuximab induction chemotherapy (phase I portion)
Phase:
Phase 2
Details
Lead Sponsor:
University of Chicago
Collaborator:
Novartis Pharmaceuticals
Treatments:
Albumin-Bound Paclitaxel
Cetuximab
Cisplatin
Everolimus
Paclitaxel
Sirolimus