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Clinical Trial Summary

The phase II clinical study is to investigate the safety, tolerability, efficacy and pharmacokinetics of ICP-022.


Clinical Trial Description

Safety, tolerability evaluation, and anti-tumor effects of ICP-022 in Chinese patients with Recurrent/Refractory Central Nervous System Lymphoma (PCNSL) and Recurrent/Refractory Secondary Central Nervous System Lymphoma (SCNSL) will be evaluated in approximately 82 subjects. Pharmacokinetics of ICP-022 will be evaluated in approximately 20 subjects . ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04438044
Study type Interventional
Source Beijing InnoCare Pharma Tech Co., Ltd.
Contact
Status Active, not recruiting
Phase Phase 2
Start date June 18, 2019
Completion date December 31, 2023

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