The rezpegaldesleukin trial reports a 61% EASI improvement. The placebo arm improved 31%.
That placebo response is not noise, and it is not unique to this trial — it is a consistent feature of atopic dermatitis studies. Trial participants use emollients more diligently, are seen regularly, are observed, and enter trials during a flare, which means regression to the mean works in the treatment's favour. Half of the headline improvement here happened in people receiving no active drug.
The consequence is practical. A patient told that a drug produces a 61% improvement will expect that improvement, and the honest figure to quote is the 30-point difference — what the drug adds beyond attention, emollients and time. Single-arm evidence and open-label extensions in this condition should be read with the same suspicion.
The habit generalises to any condition that flares and remits: eczema, psoriasis, migraine, inflammatory bowel disease. Wherever the natural history includes spontaneous improvement, the placebo arm is measuring something real, and the treatment effect is only what exceeds it.
- Atopic dermatitis placebo arms routinely improve 25 to 35%
- Quote the between-group difference to patients, not the treatment-arm change
- Trial entry during a flare guarantees regression to the mean
- Open-label extensions carry the whole placebo effect uncontrolled
- Same caution applies to any relapsing-remitting condition
The statistics, in plain English
A placebo response combines three separable things: true placebo effect, regression to the mean from enrolling during a flare, and co-interventions like emollients that both arms receive. Randomisation subtracts all three from the treatment estimate, which is why the between-group difference is the only number that isolates the drug.
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