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Clinical Trial Summary

This is a Phase I/Ⅱ, multicenter, open-label, dose-escalation study designed to evaluate the safety, tolerability, pharmacokinetics (PK), pharmacodynamics(PD) and efficacy of a novel asymmetric trivalent tri-specific humanized antibody, MBS314, administered by intravenous (IV) infusion in participants with relapsed or refractory multiple myeloma. This entry-to-human study is divided in 2 parts: a dose escalation part (Phase Ⅰa) and an expansion part (Phase Ⅰb/Ⅱ).


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT06232096
Study type Interventional
Source Beijing Mabworks Biotech Co., Ltd.
Contact Lugui Qiu, Doctor
Phone 0086-022-23608560
Email Qiulg@ihcams.ac.cn
Status Recruiting
Phase Phase 1/Phase 2
Start date February 22, 2024
Completion date March 2028

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