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(See the blog.) The NIHs RECOVER Initiative for long COVID demonstrated great initiative by using patient and physician reports to initiate a GLP-1 agonist
If the FDA finds even a minor sterility issue at your facility, a manufacturer can use that to argue in court that your entire compounded GLP-1 line is unsafe and unapproved
It wastes time, resources, and most importantly, the valuable peptide itself
There are currently around 54 million patients with a diagnosis of dementia worldwide with incidence rates predicted to triple internationally to 152 million people by 2050 and will cost health services $2 trillion a year by 2030 as per the World Alzheimer Report 2018 [3]
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