Atopic Dermatitis Clinical Trial
Official title:
Effects of Interleukin (IL)-4/IL-13 Blockade on the Structure and Function of Cutaneous Sensory Nerves: An Open-label, Single-arm Longitudinal Study With Dupilumab
24-week, open-label, single-arm longitudinal study of patients with AD, including a
comparison between baseline values for adult patients with moderate-to-severe AD and
untreated normal control patients.
Patients with AD: ≤24 to 29 weeks, including the screening period Normal control patients: ≤2
days to 5 weeks, including the screening period.
Patients with AD: adults with moderate-to-severe AD whose disease cannot be adequately
controlled with topical medications or for whom topical treatment is medically inadvisable
(eg, intolerance, other important side effects or safety risks)
Normal control patients: adults without AD or other atopic disease
n/a
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