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Clinical Trial Summary

Expected to complete 7 to 18 evaluable subjects (patients with advanced solid tumors),3 dose groups.A modified "3+3" dose-escalation design is utilized,This includes both accelerated dose escalation and traditional "3+3" dose escalation.The first dose group is accelerated titration,The first dose group is an accelerated titration of 1 to 6 evaluable subjects;The second and third dose groups are based on the traditional "3+3" dose-escalation principle,The second and third dose groups are based on the traditional "3+3" dose-escalation principle, with 3 to 6 evaluable subjects enrolled respectively.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT06144671
Study type Interventional
Source Grit Biotechnology
Contact Yongsheng Wang, PHD
Phone +86 18980602258
Email wangys@wchscu.cn
Status Recruiting
Phase Phase 1/Phase 2
Start date September 13, 2023
Completion date September 13, 2026

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