drugset / Trial / NCT02881138

A Study of RC48-ADC in Subjects With HER2-Positive Advanced Malignant Solid Tumors

NCT02881138

Phase 1 Completed 24 enrolled RemeGen Co., Ltd.
NaSingle-groupOpen-labelTreatment

Summary

A Phase I Study to Evaluate the Safety,Tolerability and Pharmacokinetics of RC48-ADC for Injection in Subjects With Advanced Malignant Solid Tumors With HER2-positive

Timeline

Start
2016-03-01
Primary completion
2020-04-30
Completion
2020-07-15

Drugs

EvaluationDrugModalityDoseRoute
Subject Disitamab Vedotin Monoclonal antibody 0.5 mg/kg
Subject Disitamab Vedotin Monoclonal antibody 1 mg/kg
Subject Disitamab Vedotin Monoclonal antibody 1.5 mg/kg
Subject Disitamab Vedotin Monoclonal antibody 2 mg/kg
Subject Disitamab Vedotin Monoclonal antibody 2.5 mg/kg

Indications