127TiP Phase II, open-label study to evaluate the safety and efficacy of praluzatamab ravtansine (CX 2009) in metastatic HR-positive/HER2 non-amplified breast cancer (mHR+/HER2− BC) and CX-2009 as monotherapy and in combination with pacmilimab in metastatic triple-negative breast cancer (mTNBC)

Abstract

Probody® therapeutics (Pb-Tx) are masked antibodies designed to be conditionally activated in the tumor microenvironment by tumor-associated proteases. This allows Pb-Tx to address previously undruggable targets (eg, CD166) that are highly expressed in both tumor and normal tissue. CX-2009 is a Probody drug conjugate of a masked anti-CD166 monoclonal antibody conjugated to DM4. A phase I CX-2009 monotherapy study showed safety and durable clinical activity (clinical benefit rate at 24 weeks [CBR24] 35%) in patients (pts) with mHR+/HER2− BC or mTNBC.