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Clinical Trial Summary

This study is a non-randomized, open-label, phase I dose-finding and dose-expansion study to evaluate the safety, tolerability, antitumor efficacy, PK and immunogen of F527 in patients with relapsed or refractory lymphoma sexual characteristics.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT05293028
Study type Interventional
Source Shandong New Time Pharmaceutical Co., LTD
Contact Shaohong Yin
Phone 86-15265901803
Email yinshaohong@lunan.com.cn
Status Not yet recruiting
Phase Phase 1
Start date May 20, 2022
Completion date May 20, 2024

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