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Clinical Trial Summary

This is an open-label phase 1 study to determine the safety and tolebility of oral ABSK021 in patients with advanced solid tumor as well as the Recommended Phase 2 dose (RP2D) of oral ABSK021. Preliminary antitumor activity will also be assessed.


Clinical Trial Description

The study will start with a dose escalation part of single-agent ABSK021 administered in repeated 28-day cycles in patients with advanced solid for safety and tolerability. The expansion part of oral ABSK021 at recommended dose of expansion (RDE) will be followed for further evaluating safety and tolerability among selected tumor types. Preliminary antitumor activity will also be assessed. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04192344
Study type Interventional
Source Abbisko Therapeutics Co, Ltd
Contact YUAN LU
Phone +86-21-68910052
Email clinical@abbisko.cn
Status Recruiting
Phase Phase 1
Start date January 20, 2020
Completion date December 31, 2023

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