drugset / Trial / NCT05144841

A Study to Evaluate Zilovertamab Vedotin (MK-2140) for Relapsed or Refractory Diffuse Large B-Cell Lymphoma (DLBCL) (MK-2140-004)

NCT05144841

Phase 2 Completed 140 enrolled Merck Sharp & Dohme LLC
Non-randomizedParallel-groupOpen-labelTreatment

Summary

The purpose of this study is to evaluate zilovertamab vedotin with respect to objective response rate and duration of response per Lugano Response Criteria as assessed by blinded independent central review (BICR). Safety and tolerability will also be evaluated in this Phase 2, single arm, interventional study.

Timeline

Start
2022-01-08
Primary completion
2026-04-21
Completion
2026-04-21

Drugs

EvaluationDrugModalityDoseRoute
Subject Zilovertamab vedotin Unknown 2.25 mg/kg Intravenous
Subject Zilovertamab vedotin Unknown 2.5 mg/kg Intravenous