Myeloma and Related Diseases Registry (MRDR)

The MRDR has reached 4,000 patients registered!!! - an incredible achievement that wouldn't be possible without the support, commitment and great work of participants, site staff and collaborators. Thank you to everyone who has helped make this happen - we look forward to sharing many more milestones with you.

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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.
4155

Patients accrued

2796

Patients with multiple myeloma

51

Number of approved sites

492

Biobank participants

Latest news

APAC MRDR funding for $5.3 million approved
16 Nov 2020

$5.3 million funding over 5 years approved for APAC MRDR

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4000 participants!!!
02 Oct 2020

The MRDR has reached 4000 patients registered!

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MRDR webinar at National Myeloma Workshop: 5 Sept
10 Aug 2020

We invite you to the free MRDR webinar: 5 Sept, 4-5pm

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My-PROMPT trial published!
05 Apr 2020

Real-time feedback of patient-reported outcomes feasible for patients and clinicians!

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Participating organisations