drugset / Trial / NCT03524326

Testing Lenvatinib and Cetuximab in Patients With Advanced Head and Neck Squamous Cell Carcinoma and Cutaneous Squamous Cell Carcinoma

NCT03524326

Phase 1 Completed 24 enrolled Memorial Sloan Kettering Cancer Center
NaSingle-groupOpen-labelTreatment

Summary

This is a phase I study, which tests the safety of different doses of lenvatinib in combination with cetuximab, to see which dose is the safest in people. This study will help find out if lenvatinib and cetuximab is a safe and useful combination for treating patients with HNSCC and cSCC.

Timeline

Start
2018-04-30
Primary completion
2022-10-13
Completion
2022-10-13

Drugs

EvaluationDrugModalityDoseRoute
Subject Cetuximab Monoclonal antibody 500 mg/m2 Intravenous
Subject Lenvatinib Small molecule 4 mg Oral
Subject Lenvatinib Small molecule 10 mg Oral
Subject Lenvatinib Small molecule 14 mg Oral
Subject Lenvatinib Small molecule 20 mg Oral
Subject Lenvatinib Small molecule 24 mg Oral