A Non-interventional, Observational Post-marketing Registry of Patients Treated With Revlimid (Lenalidomide) in Taiwan

N/ACompletedNCT01752075

Celgene100 enrolled

Overview

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)

Study Type

OBSERVATIONAL

Enrollment

100

Conditions

Multiple Myeloma

Interventions

RevlimidDRUG

The prescribing physician should prescribe and monitor REVLIMID therapy according to the guidance and recommended schedules given in the approved Taiwan package insert (PI).

Eligibility

Sex: ALLMin age: 18 Years

Medical Language ↔ Plain English

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.

Locations (1)

NTUH

Taipei, Taiwan

Outcomes

Primary Outcomes

Adverse Events

Number of participants with adverse events

Time frame: Up to two years

Secondary Outcomes

Efficacy

Revlimid dosage, reason for Revlimid discontinuation

Time frame: Up to two years

Data from ClinicalTrials.gov

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