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Clinical Trial Summary

This study aims to evaluate alternative dosing regimens of single-agent belantamab mafodotin in participants with relapsed or refractory multiple myeloma (RRMM) to determine if an improved overall benefit/risk profile can be achieved by modifying the belantamab mafodotin dose, schedule, or both.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT05064358
Study type Interventional
Source GlaxoSmithKline
Contact
Status Active, not recruiting
Phase Phase 2
Start date March 3, 2022
Completion date February 10, 2025

See also
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