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Clinical Trial Summary

This study is a Multi-center, Open-label Phase 1 Study to Determine the Recommend Phase 2 Dose (RP2D) and Evaluate PK/PD and preliminary Efficacy of HQP1351 in Patients With GIST or Other Solid Tumors.


Clinical Trial Description

The primary objective of this phase 1 study is to determine the RP2D of HQP1351 in patients with GIST or other solid tumors. The secondary objective is to assess the safety, tolerability, PK and preliminary anti-tumor activities of HQP1351 in Patients With GIST or Other Solid Tumors. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03594422
Study type Interventional
Source Ascentage Pharma Group Inc.
Contact Yifan Zhai, M.D., Ph.D.
Phone +86-20-28069260
Email yzhai@ascentagepharma.com
Status Recruiting
Phase Phase 1
Start date July 11, 2018
Completion date December 31, 2026

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