drugset / Trial / NCT05338957

A Study of MRG002 in the Treatment of Patients With HER2-expressed Advanced Malignant Solid Tumors.

NCT05338957

Phase 1/2 Unknown 30 enrolled Shanghai Miracogen Inc.
NaSingle-groupOpen-labelTreatment

Summary

The objective of this study is to assess the safety and tolerability of MRG002 in combination with HX008 in patients with HER2-expressed advanced malignant solid tumors; and to , explore the maximum tolerated dose (MTD), and to determine the recommended phase II dose (RP2D) of combination therapy; , and to evaluate the preliminary efficacy, pharmacokinetics, and immunogenicity of combination therapy in the targeted study population.

Timeline

Start
2022-08-05
Primary completion
2024-06
Completion
2024-12

Drugs

EvaluationDrugModalityDoseRoute
Subject Pucotenlimab Monoclonal antibody 3 mg/kg Intravenous
Subject TRASTUZUMAB VEDOTIN Unknown 1.8 mg/kg Intravenous
Subject TRASTUZUMAB VEDOTIN Unknown 2.2 mg/kg Intravenous
Subject TRASTUZUMAB VEDOTIN Unknown 2.6 mg/kg Intravenous

Indications