From the Desk of Dr. Danielle Meadows
Vice President of Research Programs & Operations

The four major stages of the research process that I’ve laid out in previous messages are generally applicable to any given clinical research study. But sometimes, this process can be almost cyclical rather than standalone, which is the case for the new project I want to introduce today.
At OMF’s Collaborative Center at Montreal, Dr. Moreau has built an interconnected research portfolio, where his work on one project feeds into another. In this case, his work on REMEDIAL is leading into this new study, MEDUSA, where he’s taking a precision medicine approach to trying to find effective treatments for ME/CFS.
The Heart of the Matter
- OMF’s Collaborative Center at Montreal recently launched a new study called Myalgic Encephalomyelitis Adaptive Therapeutic Solution Platform (MEDUSA).
- The first phase of MEDUSA will identify therapeutic targets based on deep phenotyping of people with ME/CFS.
- The study team will then identify FDA-approved drugs that can be repurposed against those therapeutic targets in pilot trials, following a precision medicine approach.
- Each of MEDUSA’s pilot trials will start the first stage of the research process, “Study Design and IRB/Ethics Review”, while the first phase is still ongoing.

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Myalgic Encephalomyelitis Adaptive Therapeutic Solution Platform (MEDUSA)
The Open Medicine Foundation’s Collaborative Center at Montreal, directed by Dr. Alain Moreau, recently launched a new study called Myalgic Encephalomyelitis Adaptive Therapeutic Solution Platform (MEDUSA). The overarching goal of MEDUSA is to explore therapeutic targets and promising treatments for ME/CFS using a precision medicine approach.
MEDUSA consists of a couple of phases. The first phase will involve deep phenotyping of people with ME/CFS to identify therapeutic targets. In the context of MEDUSA, deep phenotyping includes health questionnaires, testing on blood and urine samples, microRNA profiling, and cognitive testing. Then, the study team will conduct pilot trials of FDA-approved drugs that can be repurposed as interventions for those therapeutic targets.
In initial work on MEDUSA phase 1, started as part of the center’s REMEDIAL study, the team found that elevated sphingomyelin phosphodiesterase acid like 3B (SMPDL3B) was correlated with symptom severity and is associated with immune dysregulation. They are exploring therapeutic approaches for a pilot trial based on these preliminary findings.
The results of phase 1 ultimately contribute to the study design, the first stage of the research process, of MEDUSA pilot trials.

Each pilot trial resulting from phase 1 will undergo review by the Research Ethics Board in Canada in parallel with continued work on phase 1.
You can find more about this study on our website.
If you would like to be considered for participating in research opportunities like this, please consider joining our OMF StudyME Registry.