Multiple Myeloma Clinical Trial
Official title:
A Non-interventional, Observational Post-marketing Registry of Patients Treated With Revlimid (Lenalidomide) in Taiwan
The REVLIMID Registry will provide safety data from a large cohort of Taiwanese patients treated with REVLIMID. In addition, the registry will provide efficacy data and outcomes in a real-world setting (versus a clinical trial).
The REVLIMID Registry is a prospective, multi-center, observational study. The registry will
register 100 patients being prescribed REVLIMID in Taiwan during and patients will be
followed for two years after the enrollment of the last patient.
Safety and efficacy data will be recorded in the registry monthly or bi-monthly. In
accordance with the Risk Minimization Program for REVLIMID (RevAssure) a patient categorized
as a woman of childbearing potential will be prescribed REVLIMID on a monthly basis, whereas
women of non-childbearing potential and men will be allowed up to two months supply per
prescription.
After entry of baseline data, the prescribing physician should prescribe and monitor REVLIMID
therapy according to the guidance and recommended schedules given in the approved Taiwan
package insert (PI)
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|---|---|---|---|
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