drugset / Trial / NCT01927341

Phase Ib/II Study of Efficacy and Safety of MEK162 and Panitumumab, in Adult mCRC Patients With Mutant or Wild-type RAS Tumors

NCT01927341

Phase 1/2 Completed 53 enrolled Pfizer
Non-randomizedSingle-groupOpen-labelOther

Summary

The primary purpose of the phase Ib is to estimate the MTD/RPD2 and of the phase II is to assess the anti-tumor activity of MEK162 in combination with panitumumab.

Timeline

Start
2013-11-19
Primary completion
2016-01-25
Completion
2016-01-25

Drugs

EvaluationDrugModalityDoseRoute
Subject Binimetinib Small molecule 45 mg Oral
Subject Panitumumab Monoclonal antibody 6 mg/kg Intravenous

Indications