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Clinical Trial Summary

This is a Phase 1, randomized, placebo-controlled study, enrolling approximately 38 healthy adult subjects (18-65 yrs). The purpose of this study is to evaluate the safety, tolerability and PK of single ascending dose of 9MW1911 administered intravenously (IV) in healthy adult volunteers. All subjects will be followed up for safety from the time of Informed Consent through 113 days post dose.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT05170243
Study type Interventional
Source Mabwell (Shanghai) Bioscience Co., Ltd.
Contact
Status Completed
Phase Phase 1
Start date January 21, 2022
Completion date October 28, 2022

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