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Clinical Trial Summary

This study is a one-arm, open, multicenter phase 1b/2 clinical trial of PE0116combined with PE0105 in patients with Advanced Solid Tumors, aiming at exploring the MTD and RP2D and observing the preliminary efficacy.The trial can be divided into two parts: dose escalation part and expansion part.PE0105 is administered as a fixed-dose intravenous injection(3mg/kg Q3w).


Clinical Trial Description

Phase Ib This is a dose escalation,3+3 design study, to evaluate the safety and tolerability, and to determine the RP2D of PE0116 injection in patients with advanced solid tumors. One cycle is 21 days. Phase II This is an expansion phase in patients with advanced solid tumors such as ovarian cancer, cervical cancer, renal cancer, head and neck cancer to further evaluate the safety, tolerability and preliminary anti-tumor activity of PE0116 injection at the RP2D combined with PE0105 injection every three weeks. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT06026501
Study type Interventional
Source Shanghai YingLi Pharmaceutical Co. Ltd.
Contact Hanying Bao, PhD
Phone 86 21-51370693
Email hybao@yl-pharm.com
Status Not yet recruiting
Phase Phase 1/Phase 2
Start date August 31, 2023
Completion date December 31, 2027

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