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Clinical Trial Summary

This is a multi-center, open-label, Phase 1/2 study in China to evaluate the safety, tolerability, efficacy, pharmacokinetics, pharmacodynamics and immunogenicity of CM336 in patients with relapsed or refractory multiple myeloma. This study consists of a dose escalation part (Phase 1) and a dose extension part (Phase 2 ). The safety and tolerability of CM336 will be evaluated in Phase 1 study, as well as the maximum tolerated dose (MTD) and the recommended dose level for Phase 2 study will be determined. The efficacy of CM336 will be evaluated in Phase 2 study.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT05299424
Study type Interventional
Source Keymed Biosciences Co.Ltd
Contact
Status Not yet recruiting
Phase Phase 1/Phase 2
Start date April 15, 2022
Completion date December 2026

See also
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