SURMOUNT-4 was built to answer the stopping question, and it did
The regain trajectories, arm by arm, with the estimands named.
TheCompound Journal
Reporting on incretins, compounding & the peptide supply chain
Every issue published in 2026 to date — 6 numbers, 1,020 pieces.
The regain trajectories, arm by arm, with the estimands named.
Duplicate submissions under different names test within-laboratory repeatability, which is a different quantity from between-laboratory reproducibility.
We set out the questions that distinguish a symptom to manage from a dose to change.
This is the single interaction with ordinary medical care that patients most need to disclose, and it is the one most often not asked about.
Aggregates dissociate in the mobile phase and are recorded as monomer. Only a size-based separation reports them.
Three randomised withdrawal designs have tested what happens when treatment stops. Their results are consistent and they are consistently misreported.
A plateau at an intermediate dose and a plateau at the maximum dose look identical from the outside and mean different things.
Calibration drift is real, unremarkable, and the reason serious laboratories run internal standards.
The argument for a baseline panel is that it makes every subsequent result interpretable. The argument against frequent monitoring is that noise accumulates faster than…
Four independent services underpin confidence in this market. All four are competent at chemistry. Microbiology is a different accreditation, a different facility and a…
The clinical effect profile is almost fully predictable from where the receptor is expressed, which is unusual and useful.
What adding GIP activity does, on the current evidence, and what remains unresolved.
Gradient slope is the single most consequential method parameter for a reported purity figure, and it is the one most often omitted.
The evidence base is one secondary analysis, several small studies and a large amount of extrapolation from bariatric surgery.
Real-world persistence figures, with their definitions stated, because the definitions are doing most of the work.
An effect is dose-limiting when it prevents adequate intake, prevents normal activity, or produces a risk of its own. Discomfort alone is not the test.
Calibration drift is real, unremarkable, and the reason serious laboratories run internal standards.
A robust, cheap, standardised assay with a specific and well-catalogued set of failure modes, several of which are common in this population.
The absence of microbiological capability in this market is a commercial fact with a straightforward explanation, and it is worth understanding before blaming anybody for it.
What scintigraphy and breath-test studies established about emptying rate, and what they did not.
The central effects are not a bonus. On the current evidence they are the principal mechanism of weight loss.
A peptide has a monoisotopic mass and an average mass, they differ by several daltons at this molecular size, and a certificate that does not say which it quotes cannot be…
Why the reason for stopping changes what happens afterwards.
The clinical effect profile is almost fully predictable from where the receptor is expressed, which is unusual and useful.