STEP 1 misses on a secondary endpoint the coverage has not mentioned
A design note rather than a result: what the comparator was, and what that permits you to conclude.
TheCompound Journal
Reporting on incretins, compounding & the peptide supply chain
Dispatches Dispatch
Reported from the sessions, and from the two hours afterwards.
Across 11 presentations at a congress in Wuxi this month, one theme recurred with a persistence that the programme did not anticipate: duration. Not whether these drugs work, which nobody in the room disputed, but for how long they will be taken, by whom, and who pays for the twentieth year.
Of the 11 presentations the Journal attended, 8 addressed treatment duration or discontinuation directly. Two reported registry data on persistence at twelve and twenty-four months, both showing attrition substantially higher than trial discontinuation rates, and both attributing the majority of it to cost and coverage rather than tolerability.
The decile plot showed the familiar picture: a long right tail of very large responses, a substantial middle, and a group with minimal change. Questions from the floor concentrated on whether anything in the baseline dataset separated the groups. The presenter’s answer was that nothing did, at least not usefully.
Congresses in this field are heavily sponsored, and the Journal pays its own registration and travel. Where a session was industry-supported we say so, because the sponsorship shapes the programme even where it does not shape the data.
"I see patients with unlabelled vials every month and there is no guidance anywhere that tells me what to do," said Dr Farida Al-Mansouri, internal medicine physician, Doha. "That session was the first time I have heard it discussed at a podium."
"I see patients with unlabelled vials every month and there is no guidance anywhere that tells me what to do," said Dr Rafał Sikorski, toxicologist, Medical University of Warsaw. "That session was the first time I have heard it discussed at a podium."
Unpublished congress material is flagged as unpublished in our trial-data explorer and is removed if it is not published within eighteen months.
Congress abstracts are not peer-reviewed. Nothing in this item is clinical advice.
A design note rather than a result: what the comparator was, and what that permits you to conclude.
Reported from the sessions, and from the two hours afterwards.
Efficacy was never the question in this appraisal. Duration of treatment was.
Reported from the sessions, and from the two hours afterwards.
Reported from the sessions, and from the two hours afterwards.
Reported from the sessions, and from the two hours afterwards.