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Clinical Trial Summary

This is a phase I, multi-center, open-label, dose escalation study to evaluate the safety, tolerability, pharmacokinetics and clinical activity of LP-118 in patients with advanced malignancies, including solid tumors and B-cell lymphomas. LP-118 is a BCL-2/BCL-XL small molecule inhibitor.


Clinical Trial Description

LP-118 is an oral selective BCL-2 inhibitor with tuned BCL-XL activity, aiming to improve antitumor efficacy and reduce the risk of thrombocytopenia. Clinical development of LP-118 includes targeting of relapsed or refractory hematological malignancies and solid tumors. This is a multi-center, open-label, Phase 1 dose escalation study of LP-118 in patients with advanced malignancies, including advanced/metastatic solid tumors and relapsed/refractory B-cell lymphomas, to determine the safety, tolerability, pharmacokinetics profile and preliminary anti-tumor efficacy. Upon completion of the Phase 1 dose escalation study and establishment of maximum tolerated dose (MTD) and recommended phase 2 dose (RP2D), the dose expansion study will be implemented in patients with protocol designated type of disease. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05025358
Study type Interventional
Source Guangzhou Lupeng Pharmaceutical Company LTD.
Contact Yue Shen, PhD
Phone 86571-81999616
Email [email protected]
Status Recruiting
Phase Phase 1
Start date September 14, 2021
Completion date July 30, 2024

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