Clinical perspective, offered as context rather than as advice. Start from the measurement rather than the conclusion. Almost every disagreement here turns out to be two people measuring different things and comparing the numbers anyway.
wendy_avl said:The boring version of this is the one that works, and the boring version is: measure a baseline, change one variable, wait, measure again under the…
Coming at wendy_avl’s question from a different direction. The version of this that has an answer is narrower than the version being asked. Narrow it and it becomes tractable; leave it broad and the thread will produce nine confident and incompatible replies.
One concrete data point for the thread. The dose-response is real but shallow at the top. Across STEP 1 and STEP 4 the gap between 1.7mg and 2.4mg is a couple of percentage points of body weight on average, and the average is carrying a wide spread — plenty of people at 1.7mg sit above the 2.4mg mean. If a dose is working and tolerable, "working" is the relevant variable, not "maximal".
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Browse GL BiochemFollowing on from wendy_avl — and this may be the naive question:
How much of the between-person variation is pharmacokinetic and how much is just adherence measured badly?