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Clinical Trial Summary

The study aims to evaluate the efficacy and safety of IAH0968 in combination with gemcitabine and cisplatin for the treatment of HER2-positive unresectable advanced/metastatic malignant tumors and cholangiocarcinoma. The study is divided into two stages: Phase Ib, an open-label, non-randomized, multicenter dose-escalation trial, and Phase II, a randomized, double-blind, parallel-controlled, multicenter trial.


Clinical Trial Description

Phase Ib is an open-label, non-randomized, multicenter dose-escalation trial. It utilizes the classic "3+3" design to investigate the safety and tolerability of IAH0968 in combination with gemcitabine and cisplatin for the treatment of HER2-positive unresectable advanced/metastatic malignant tumors and cholangiocarcinoma. Phase II study is a randomized, double-blind, parallel-controlled, multicenter research design. It aims to investigate the efficacy of IAH0968 in combination with gemcitabine and cisplatin for the treatment of HER2-positive unresectable advanced/metastatic malignant tumors and cholangiocarcinoma. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05991518
Study type Interventional
Source SUNHO(China)BioPharmaceutical CO., Ltd.
Contact cao jianxiang, M.D.
Phone 18018039840
Email caojianxiang@sunho-bio.com
Status Recruiting
Phase Phase 1/Phase 2
Start date April 25, 2023
Completion date December 2025

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