This real-world, multicenter prospective clinical study is designed to apply our internationally developed prognostic scoring system to guide individualized therapy in +1q newly diagnosed multiple myeloma (NDMM), using minimal residual disease (MRD) status as the primary endpoint.
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MRD negativity rate
Timeframe: through study completion, up to 2 years
sustained MRD negativity rate
Timeframe: through study completion, up to 2 years
Progression-Free Survival (PFS)
Timeframe: through study completion, up to 2 years
Overall Survival (OS)
Timeframe: through study completion, up to 2 years
objective response rate
Timeframe: through study completion, up to 2 years
Treatment related adverse event(TRAE)
Timeframe: through study completion, up to 2 years