DUPIlumab Dose REDUCtion in Patients With Controlled Atopic Eczema

Recruiting Phase 4 Interventional Study
Atopic Dermatitis Atopic Dermatitis Eczema
No Placebo Group Every participant receives an active treatment — no one gets a placebo. Prior Safety Data This treatment has already been tested in at least one earlier human trial.
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At a Glance
Age
18 and older
Sex
Any
Trial phase
Phase 4
Study type
Interventional
Purpose
Treatment
Participants needed
216 (estimated)
Sponsor
Academisch Medisch Centrum - Universiteit van Amsterdam (AMC-UvA) · Other
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About This Trial
The goal of this randomized controlled trial is to study the (cost)effectiveness of extending the intervals between dupilumab doses in patients with well-controlled atopic eczema, while considering physician- and patient-reported disease severity, quality of life, and dupilumab serum trough levels. Patients will be divided randomly into three groups, receiving dupilumab 300 mg every 2 weeks, every…
Trial Locations
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Eligibility Criteria
Inclusion Criteria: * The subject is an adult, * Has a diagnosis of AE, * Receives dupilumab 300 mg q2w for the treatment of AE, * Has controlled disease according to the Treat-to-Target criteria, * Agrees to the possibility that the dosage of dupilumab will be lowered, * Has voluntarily signed and…
Contacts

Phyllis I Spuls, MD PhD

+3120 566 9111

ph.i.spuls@amsterdamumc.nl

CONTACT

Anouk GM Caron, MD

+31653704573

a.caron@amsterdamumc.nl

CONTACT