drugset / Trial / NCT04934514

Clinical Study of IAH0968 in Patients With HER2-positive Advanced Solid Tumors

NCT04934514

Phase 1/2 Unknown 97 enrolled SUNHO(China)BioPharmaceutical CO., Ltd.
Non-randomizedSequentialOpen-labelTreatment

Summary

This is a phase I/IIa study to evaluate the safety, tolerability and preliminary efficacy of IAH0968 in patients with HER2-positive advanced solid tumors who have failed standard treatment.

Timeline

Start
2021-07-06
Primary completion
2024-12-31
Completion
2025-03-31

Drugs

EvaluationDrugModalityDoseRoute
Subject IAH0968 Monoclonal antibody 6 mg/kg
Subject IAH0968 Monoclonal antibody 10 mg/kg
Subject IAH0968 Monoclonal antibody 15 mg/kg
Subject IAH0968 Monoclonal antibody 20 mg/kg
Background Cisplatin Other / unclassified 75 mg/m2 Intravenous
Background Gemcitabine Small molecule 1000 mg/m2 Intravenous

Indications