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Clinical Trial Summary

To evaluate the safety and tolerability of HMPL-653 in patients with advanced solid tumors who have failure of standard of care or can not tolerate standard of care or those with TGCT, and to determine the maximum tolerated dose (MTD) and/or the recommended phase II clinical study dose (RP2D) of HMPL-653 in patients with advanced solid tumors.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT05277454
Study type Interventional
Source Hutchison Medipharma Limited
Contact Cindy Hua
Phone +86 21 2067 3221
Email cindyh@hutch-med.com
Status Recruiting
Phase Phase 1
Start date January 18, 2022
Completion date April 14, 2025

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