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Clinical Trial Summary

It is a multi-center, prospective, open-label, two-stage optimized design, single-arm, phase II clinical study to evaluate the efficacy and safety of F520 for the treatment of Relapsed/Refractory Primary Central Nervous System Lymphoma (PCNSL) or Secondary Central Nervous System Lymphoma (SCNSL).


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT04457869
Study type Interventional
Source Shandong New Time Pharmaceutical Co., LTD
Contact
Status Not yet recruiting
Phase Phase 2
Start date November 1, 2020
Completion date January 1, 2023

See also
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