Last updated on December 2018

A Post Authorisation Registry of IMNOVID (Pomalidomide) for Patients With Relapsed and Refractory Multiple Myeloma.


Brief description of study

This registry is a prospective, multi-center, observational study and will collect safety data on multiple myeloma adult patients who have received at least two prior therapies and take IMNOVID (pomalidomide) as part of standard care.

The registry will remain open until 500 patients will have received at least 3 cycles of pomalidomide. All patients registered will be followed up prospectively for up to 3 years following the end of pomalidomide treatment. During this time the incidence of second primary malignancies (SPM), overall survival and any occurrence of a pregnancy will be assessed.

Clinical Study Identifier: NCT02164955

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Associate Director, Clinical Trial Disclosure

Evangelisches Krankenhaus Hamm GgmbH
Hamm, Germany
0.83miles
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Recruitment Status: Open


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