drugset / Trial / NCT03792841

Safety, Tolerability, Pharmacokinetics, and Efficacy of Acapatamab in Subjects With mCRPC

NCT03792841

Phase 1 Terminated 212 enrolled Amgen
Non-randomizedSequentialOpen-labelTreatment

Summary

A phase 1 study evaluating the safety, tolerability, pharmacokinetics, and efficacy of prostate specific membrane antigen half-life extended bispecific T-cell engager acapatamab in subjects with metastatic castration-resistant prostate cancer, and to determine the maximum tolerated dose (MTD) or recommended phase 2 dose (RP2D).

Timeline

Start
2019-02-05
Primary completion
2023-06-29
Completion
2023-06-29

Drugs

EvaluationDrugModalityDoseRoute
Subject Acapatamab Monoclonal antibody Intravenous
Subject Pembrolizumab Monoclonal antibody Intravenous
Background Etanercept Protein / enzyme biologic Subcutaneous