drugset / Trial / NCT00612703

A Phase 1 Study of ARQ 197 in Adult Patients With Advanced Solid Tumors

NCT00612703

Phase 1 Completed 32 enrolled ArQule, Inc.
Non-randomizedSingle-groupOpen-labelTreatment

Summary

To determine the safety, tolerability and recommended Phase 2 dose of ARQ 197 when administered in combination with erlotinib to patients with advanced solid tumors

Timeline

Start
2008-02
Primary completion
2010-09
Completion

Drugs

EvaluationDrugModalityDoseRoute
Subject Tivantinib Small molecule 120 mg Oral
Subject Tivantinib Small molecule 240 mg Oral
Subject Tivantinib Small molecule 360 mg Oral
Subject Tivantinib Small molecule 480 mg Oral
Background Erlotinib Small molecule 150 mg

Indications