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Clinical Trial Summary

This is a phase I, open-label, multi-center, non-randomized, 2-part first time inhuman (FTIH) study for SYHA1807. Part 1 is a dose escalation phase to determine the recommended phase 2 dose (RP2D) for SYHA1807 based on the safety, tolerability and pharmacokinetics (PK) profiles observed after oral administration of SYHA1807. The dose escalation study will be performed according to the 3+3 design. Once RP2D is identified, an expansion cohort (Part 2) of up to 12~40 subjects will be enrolled to further evaluate the clinical activity and tolerability of SYHA1807 in subjects with extensive-stage Small Cell Lung Cancer (SCLC).


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT04404543
Study type Interventional
Source CSPC ZhongQi Pharmaceutical Technology Co., Ltd.
Contact Kun Lou
Phone 031167808817
Email loukun@mail.ecspc.com
Status Not yet recruiting
Phase Phase 1
Start date June 1, 2020
Completion date June 30, 2021

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