Actively Recruiting

Age: 6Years - 99Years
All Genders
ID06387654

Constitution of a Collection of Biological Samples for Clinical and Physiopathological Study of Autoimmune, Dysimmune, or Auto-inflammatory Dermatological Diseases

Led by University Hospital, Toulouse · Updated on 2026-03-17

800

Participants Needed

1

Research Sites

260 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

This research aims to collect biological and clinical data from patients with autoimmune, dysimmune, or auto-inflammatory skin diseases. These conditions include a wide range of rare diseases that collectively affect a significant portion of the adult population, especially women. The study focuses on understanding the breakdown of self-tolerance and the complex mechanisms behind these diseases, as well as identifying patient subgroups based on clinical and biological profiles to improve diagnosis and treatment. Participants will provide biological samples such as blood, cerebrospinal fluid, saliva, stools, urine, tissue biopsies, and hair follicles during their normal diagnostic and follow-up care. The study will gather these samples and clinical data over an average period of one year. The goal is to build a collection that supports the identification of new autoantibodies, biomarkers related to disease severity, and the exploration of disease mechanisms. Samples will also be analyzed to compare blood cell populations before and after certain therapies. During the study, participants will be involved in providing biological specimens as part of their routine medical care. Researchers will monitor these samples and clinical data to assess disease markers, treatment responses, and underlying disease processes. The main outcome is the development of a detailed biological and clinical collection to support future research and therapeutic strategies. The study follows participants for about one year, with ongoing data collection throughout this period.

CONDITIONS

Brief Title

Clinico-biological Collection of Autoimmune, Dysimmune or Auto-inflammatory Dermatological Diseases

Who Can Participate

Age: 6Years - 99Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Skin damage of documented or probable autoimmune, dysimmune, or auto-inflammatory origin
  • Patients with autoimmune bullous dermatoses such as pemphigus or pemphigoid
  • Patients with systemic autoimmune diseases associated with skin damage like lupus, scleroderma, or dermatomyositis
  • Patients with cutaneous lupus
  • Patients with dysimmune skin diseases such as psoriasis or eczema
  • Patients with immuno-induced dermatological disorders or drug-related dermatitis
  • Patients receiving or likely to receive new therapies including new molecules, checkpoint inhibitors, gene therapy, or cell therapy
  • Patients with suspected autoimmune, dysimmune, or auto-inflammatory dermatological damage
  • Adults and children aged 6 years and older
Not Eligible

You will not qualify if you...

  • Patients under legal protective supervision such as guardianship or curatorship
  • Patients younger than 6 years old
  • Pregnant or breastfeeding women

AI-Screening

AI-Powered Screening

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Sample Collection

Duration - Up to 1 year

Participants provide biological samples as part of their normal diagnosis and follow-up process. This includes blood samples, CSF, saliva, stools, urine, other biological fluids, tissue biopsies, and hair follicles.

Visits aligned with routine clinical care for diagnosis and follow-up

Long-term Monitoring

Duration - Up to 1 year

Participants are observed over time to collect clinical and biological data related to autoimmune, dysimmune, or auto-inflammatory dermatological diseases to support research on diagnosis, therapy, and disease mechanisms.

Ongoing assessments during routine care visits

Trial Site Locations

Total: 1 location

1

University Hospital

Toulouse, France, 31059

Actively Recruiting

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Research Team

C

Chloé BOST, MD, PhD

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

1

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