A Phase 1 Dose Escalation Study of OMP-52M51 in Subjects with Solid Tumors

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Investigator: Pamela N. Munster, MD
Sponsor: OncoMed Pharmaceuticals, Inc.

Location(s): United States

Description

This is an open-label Phase 1a dose escalation study of single-agent OMP-52M51 in subjects with relapsed or refractory solid tumors. Study includes a dose escalation phase and expansion phase. Subjects will be assessed for safety, immunogenicity, pharmacokinetics, biomarkers, and efficacy.