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CytomX Therapeutics announces first patient dosed in Phase 1 study of CX-801

CytomX Therapeutics (CTMX) announced that the first patient has been dosed with CX-801 in combination with KEYTRUDA, Merck’s anti-PD-1 therapy, in the ongoing Phase 1 dose escalation study evaluating safety and initial clinical activity in patients with metastatic melanoma. CytomX is conducting a focused Phase 1 dose escalation study of CX-801 in metastatic melanoma. The combination arm of the study evaluating CX-801 in combination with KEYTRUDA has been initiated following successful the clearance of the first three CX-801 monotherapy dose escalation cohorts.

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