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Clinical Trial Summary

The study of LVGN7409-201 is designed to use a bridging dose escalation to quickly establish the maximum tolerated dose (MTD) and/or the recommended dose for expansion (RDE) as well as the recommended Phase 2 dose(s) (RP2D) of LVGN7409 as a single agent (monotherapy) in the treatment of locally advanced, metastatic or recurrent/refractory malignancy.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT05152212
Study type Interventional
Source Lyvgen Biopharma Holdings Limited
Contact
Status Completed
Phase Phase 1
Start date September 29, 2021
Completion date December 19, 2023

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