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longer studies in disease models (for example, kidney aging) suggest benefits at defined doses, but comprehensive long-term safety pharmacology remains sparse in the public domain
What to do with results: If markers improved, you have evidence the protocol worked
There are two ways to answer this question: how long you stay on the treatment and how long you can safely keep using the physical pen
Around the same time, I think you remember that all of pharma was interested in obesity in the early 90s, everyone wanted to do diabetes as well as obesity, but they were separate teams and they all wanted to do small molecules, but it just happens to be so that the best idea we could find at that time was actually GLP-1, because we actually had clinical data relatively early that GLP-1 was a really good candidate as a treatment for diabetes because of the glucose sensitivity of the actions
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