What the new Brazil guidance says about stopping
The evidence base is thin and the document says so, which is to its credit.
TheCompound Journal
Reporting on incretins, compounding & the peptide supply chain
Page 14 of 31 of this archive, newest first.
The evidence base is thin and the document says so, which is to its credit.
Three randomised withdrawal designs have tested what happens when treatment stops. Their results are consistent and they are consistently misreported.
A small number of serious gastrointestinal events occur in people taking these drugs. Distinguishing them from the expected effect profile is the most consequential…
We work through the residual-exposure table so the decision can be made from numbers rather than from feel.
The insulin injection-technique literature is large, well conducted and directly transferable on questions of depth and tissue. We say where it stops transferring.
The clinical effect profile is almost fully predictable from where the receptor is expressed, which is unusual and useful.
The evidence base is thin and the document says so, which is to its credit.
The evidence base is thin and the document says so, which is to its credit.
The evidence base is thin and the document says so, which is to its credit.
A rotation scheme that is too complicated will not be followed. We describe the simple ones that are.
Receptor pharmacology is strong on average effects and almost silent on individual variation. That gap is where most reader questions live.
We work through the arithmetic in full, because it is short, and because the errors it prevents are order-of-magnitude errors.
The evidence base is thin and the document says so, which is to its credit.
What a slow reduction could plausibly buy, and what it certainly cannot prevent.
What the trials measured was continuation against withdrawal. What patients want to know is continuation at a lower dose, and that study has largely not been done.
Insulin syringes are graduated in units on a convention that fixes 100 units to one millilitre. That convention says nothing about how much peptide is in a unit, and…
Every major phase 3 protocol in this class allowed escalation to be delayed for tolerability. Almost no product label explains the mechanics of doing so.
The features that should prompt urgent assessment, stated once and plainly.
The receptor populations that produce satiety and the ones that produce nausea overlap substantially. That is why the ceiling of this drug class is where it is, and it is…
The evidence base is thin and the document says so, which is to its credit.