Myeloma and Related Diseases Registry (MRDR)

Helping clinicians and hospitals to provide the best possible care to people with multiple myeloma, monoclonal gammopathy of undetermined significance (MGUS), plasma cell leukaemia or plasmacytoma.

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This clinical quality registry aims to improve myeloma outcomes by providing an evidence base for the best strategies to diagnose, treat and support people with myeloma and related diseases.

What is the registry?

Learn about how the registry works and the data we collect.
Benefits

Participation in the registry provides advantages for sites and patients.
About our projects

Find out about MRDR projects and how registry data is being used.
5269

Patients accrued

3528

Patients with multiple myeloma

56

Number of approved sites

570

Biobank participants

Latest news

Rare Disease Day, Monday 28 Feb!
24 Feb 2022

Thanks to those who contribute to improving care, and providing support for people living with myeloma & related diseases!

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MRFF grant for MY-PROMPT-2 trial!
11 Jan 2022

MY-PROMPT-2 project funded!

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5000 patients registered!!
15 Dec 2021

The MRDR reached 5000 registered participants!

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Join us at the Asia-Pacific MRDR Investigators’ meeting!
10 Dec 2021

All are welcome to the Asia-Pacific MRDR Investigators' meeting, Fri, 17 Dec, 4pm AEDT!

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Participating organisations