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Clinical Trial Summary

This is an open-label, dose-escalation study of the study drug YH002. The study is designed to determine the safety, tolerability and maximum tolerated dose (MTD) and recommended Phase 2 dose (RP2D) of YH002 in patients with advanced solid Malignancies


Clinical Trial Description

This is a single arm clinical trial in subjects with advanced solid tumor receiving multiple doses of YH002 intravenously (IV). YH002 will be administered (IV) in 6-48 patients with advanced solid tumors. An accelerated titration method followed by a traditional 3+3 dose escalation algorithm will be utilized to determine MTD/MAD. Patients will be dosed at Dose A, Dose B, Dose C, Dose D, Dose E, Dose F, Dose G, and Dose H every 3 weeks (Q3W). ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04353102
Study type Interventional
Source Eucure (Beijing) Biopharma Co., Ltd
Contact
Status Completed
Phase Phase 1
Start date April 22, 2020
Completion date November 24, 2021

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