Multiple Myeloma Clinical Trial
Official title:
A Non-interventional, Observational Post-marketing Registry of Multiple Myeloma Adult Patients Treated With Revlimid (Lenalidomide) in China
The primary objective of this study is to document efficacy and safety data in a real-world setting of Chinese multiple myeloma patients who have received at least one prior therapy treated with REVLIMID (lenalidomide).
This registry is prospective, multi-center, observational study and will collect efficacy
and safety data on multiple myeloma adult patients who have received at least one prior
therapy and take REVLIMID as part of standard care associated with patients' treatment in
order to characterize the use, efficacy and outcomes of REVLIMID treatment.
The registry will capture data from 600 patients being prescribed REVLIMID in specified
hospitals and all patients will be followed in the registry for two years after enrollment
of the last patient.
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Observational Model: Cohort, Time Perspective: Prospective
Status | Clinical Trial | Phase | |
---|---|---|---|
Recruiting |
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Phase 1/Phase 2 | |
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