Evaluation of the Prevalence of BP180 and BP230 Autoantibodies in the Serum of Patients With Pruritus Under Immunotherapy

Recruiting N/A Interventional Study
Patients With Chronic Pruritus for More Than 1 Month Who Have Received Immunotherapy
No Placebo Group Every participant receives an active treatment — no one gets a placebo.
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At a Glance
Age
18 and older
Sex
Any
Study type
Interventional
Purpose
Other
Participants needed
100 (estimated)
Sponsor
University Hospital, Rouen · Other
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About This Trial

The aim of the study is to evaluate the prevalence of positive anti BP180 and/or anti BP230 serology in the serum of patients with chronic and diffuse pruritus for at least 1 month under immunotherapy and in the absence of obvious pruritic dermatosis (e.g. scabies, contact eczema...).

Trial Locations
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Eligibility Criteria
Inclusion Criteria: * Patient currently receiving immunotherapy (pembrolizumab, nivolumab, atezolizumab, durvalumab) as monotherapy or in combination OR patient who has received immunotherapy (pembrolizumab, nivolumab, atezolizumab, durvalumab) as monotherapy or in combination within the last 6 mon…
Contacts

Vivien HEBERT, MD

02 32 88

vivien.hebert@chu-rouen.fr

CONTACT

Armelle GUIDOTTI

023288

armelle.guidotti@chu-rouen.fr

CONTACT