THE MYELOMA CANADA RESEARCH NETWORK (MCRN)
  BRINGING CANADIAN-MADE TRIALS
 TO CANADIAN PATIENTS

THE MCRN'S MISSION - EXPLAINED 

1. To conduct innovative Phase I and II clinical trials and translational research in a collaborative manner to improve patient outcomes in myeloma

What this means:
The MCRN brings innovative Canadian-designed clinical trials to hundreds of patients in over 20 centres, in 9 provinces, in order to study the efficacy of new treatments that are not yet approved by Health Canada or new treatment combinations. Furthermore, the collaboration amongst the centres allows the network of researchers to leverage expertise and share findings and knowledge amongst all of the members across the country.

To highlight some of the expertise across the country:
    • Genomics (Calgary)
    • Drug target evaluation (Calgary, Toronto, Winnipeg)
    • Minimal residual disease (Toronto, Montreal)
    • Mechanisms of resistance (Calgary, Toronto)
    • Cell therapy (Montreal)
    • High-risk disease (Montreal, Calgary)
 
Research conducted in this collaborative, entrepreuneurial setting promotes the advancement of clinical research and dissemination of results at an accelerated pace in Canada.  

2. To publish evidence-based and peer-reviewed consensus statements on the diagnosis and treatment of myeloma

What this means:
Researchers can better understand how to treat and diagnose patients living with multiple myeloma, using real-world evidence. Clinical trials aim to answer questions such as: What is the optimal dosage of the treatment in question? At what frequency should the treatment be given? Does the treatment work better in combination with another drug? The answers to the questions pave the way to identifying the best treatment approaches for patients in the future through a clinical consensus, based on objective clinical trial findings. 
3. To develop a nationwide myeloma patient database
 
What this means:
Data collected in Vancouver will be shared with researchers in Halifax, and vice versa. Clinical information from all participating centres will be c ompiled and stored in a nationwide database, providing a rich bank of real-world clinical evidence, to help guide clinical decision-making and improve patient out comes. The national database will also help support public funding decisions with "real-world" data that may provide compelling clinical evidence to confirm the super iority of a novel treatment or combination. Pharmaceutical and biotechnol ogy companies, as well as public and private payers, are increasingly looking for this type of information. All data collected will be of course subject to Canadian privacy rules to ensure patient confidentiality.   
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