Multiple Myeloma
Conditions
Keywords
Multiple myeloma
Brief summary
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).
Detailed description
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)
Interventions
DRUGRevlimid
The prescribing physician should prescribe and monitor REVLIMID therapy according to the guidance and recommended schedules given in the approved Taiwan package insert (PI).
Sponsors
Celgene
Study design
Observational model
CASE_ONLY
Time perspective
PROSPECTIVE
Eligibility
Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No
Inclusion criteria
* Adult patients 18 years of age or older * Patients that are being prescribed REVLIMID in combination with dexamethasone for the treatment of multiple myeloma and that have received at least one prior therapy * Patient must be willing and able to provide informed consent * Patients will be informed about the Registry and will have to sign a specific Registry Informed Consent Form * Be able to ask questions prior to signing the Subject Information and Consent Form * Be clearly informed that their involvement/participation in the registry is voluntary * Understand that their medical care will not be altered in any way by their participation in the registry
Exclusion criteria
\- A Patient who is unwilling or unable to provide informed consent will not be included.
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Adverse Events | Up to two years | Number of participants with adverse events |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Efficacy | Up to two years | Revlimid dosage, reason for Revlimid discontinuation |
Countries
Taiwan
Outcome results
None listed