drugset / Trial / NCT06378242

To Evaluate the Safety, Efficacy, and Pharmacokinetics of Intravesical Instiliations of Disitamab Vedotin in Patients With High-risk Non-muscular Invasive Bladder Cancer (NMIBC) That Express HER2

NCT06378242

Phase 1/2 Recruiting 24 enrolled RemeGen Co., Ltd.
NaSingle-groupOpen-labelTreatment

Summary

The purpose of this study is to evaluate the safety, efficacy, and pharmacokinetics of intravesical instiliations of Disitamab Vedotin in patients with high-risk non-muscular invasive bladder cancer (NMIBC) that express HER2

Timeline

Start
2024-06-14
Primary completion
2029-03-15
Completion
2029-12-31

Drugs

EvaluationDrugModalityDoseRoute
Subject Disitamab Vedotin Monoclonal antibody 60 mg Other
Subject Disitamab Vedotin Monoclonal antibody 120 mg Other
Subject Disitamab Vedotin Monoclonal antibody 180 mg Other