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Clinical Trial Summary

This study will assess the safety and tolerability and pharmacokinetics of BH009 in patients with advanced head and neck squamous (non-nasopharyngeal) and ovarian cancer.


Clinical Trial Description

This is a multicenter, open label phase I clinical study to evaluate the safety, tolerability, and pharmacokinetic profile of BH009 in patients with advanced squamous head and neck cancer (non-nasopharyngeal) and ovarian cancer, and to initially explore its clinical effectiveness. This study will use a "3+3" dose escalation design to determine the maximum tolerated dose (MTD) and the recommended phase 2 dose (RP2D) of BH009. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT06232863
Study type Interventional
Source Zhuhai Beihai Biotech Co., Ltd
Contact Xiaohua Wei, PM
Phone 13500248359
Email xhwei@bayhibiotech.com
Status Recruiting
Phase Phase 1
Start date January 18, 2023
Completion date April 30, 2024

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