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Clinical Trial Summary

This is a study to evaluate the efficacy and safety of TQ-B3525 in subjects with relapse/refactory peripheral T-cell lymphoma who have received at least 1 lines of therapeutic schedules. TQ-B3525 tablet administered 20mg orally, once daily in 28-day cycle.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT04615468
Study type Interventional
Source Chia Tai Tianqing Pharmaceutical Group Co., Ltd.
Contact Yuankai Shi, Doctor
Phone 010-87788293
Email syuankaipumc@126.com
Status Not yet recruiting
Phase Phase 2
Start date December 1, 2020
Completion date October 31, 2022

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