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Clinical Trial Summary

This study was an open, single-arm, enriched, multicenter Phase II study.


Clinical Trial Description

The trial was divided into screening period, treatment period and follow-up period. Participants entered the screening period after signing informed consent and met the inclusion criteria. Subjects who did not meet the exclusion criteria were treated with F520 monotherapy, intravenously, at 3mg/kg every 3 weeks until disease progression or intolerable toxicity or withdrawal for other reasons, for a maximum of 2 years. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT06226350
Study type Interventional
Source Shandong New Time Pharmaceutical Co., LTD
Contact
Status Completed
Phase Phase 2
Start date March 4, 2021
Completion date January 3, 2024

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