A 44-week Monocentric Open Study Assessing the Efficacy and Safety of Deucravacitinib in Adults with Inflammatory Genodermatoses

Phase 2

Recruiting

• Conditions: Epidermolysis Bullosa Simplex; Ichthyosis; Genodermatosis; Inflammatory Congenital Ichthyoses
• Interventions: Drug: deucravacitinib

• Registration Number: NCT06136403
• Lead Sponsor: Centre Hospitalier Universitaire de Nice

Brief Summary

The goal of this clinical trial is to learn about deucravacitinib treatment in adults with inflammatory epidermal genodermatoses . The main question it aims to answer are: describe efficacity and safety of this treatment.

Participants will take treatments and have to use bullets during the study period.

Detailed Description

The patient will have 8 visits After Confirmation of inclusion criteria and no exclusion criteria, the study will be explain to the patient after signing the inform consent and be included in the study Treatment Period (Period 1); challenge period This period will be the first treatment period that will occur from 16 weeks. During this period the patient will see the doctor at the hospital, he will perform the study procedures The second period : dechallenge (period 2): All patients stop their treatment for 12 weeks.

The second treatment period - rechallenge (period 3) the patient will take the treatment for a second 16 weeks period At week 44 - End of study

At each visit:

The investigator at each visit compliance to the treatment and adverse events, Measure vital signs and perform clinical examination.

The patient will assess the different questionnaires, for the study and have blood sample

Study Timeline

• Study Start: 2023-03-18
• Study First Submitted: 2023-11-13
• Study First Submitted QC: 2023-11-13
• Study First Posted: 2023-11-18
• Status Verified: 2025-02
• Last Update Submitted: 2025-02-21
• Last Update Posted: 2025-02-24
• Primary Completion: 2025-09-30
• Study Completion: 2026-10-12

Recruitment & Eligibility

• Status: RECRUITING
• Sex: All
• Target Recruitment: 10

Inclusion Criteria

• Subject has congenital skin fragility with skin and/or mucosal blisters, a clinical phenotype of EBS-sev and a laboratory confirmed diagnosis of EBS by KRT5 and/or 14 mutation (autosomal only) OR a clinical phenotype of inflammatory ichthyosis (IC) including keratinopathic ichthyosis due to KRT1/10 mutation, ECI with identified genetic mutations (TGM5, NIPAL4, ABCA12, etc...).

• Subject has at least a mean daily number of 4 new blisters (EBS-sev) OR an ISS > 50/128.

  • Subject agrees not to use any topical therapies other than the investigator approved.

Exclusion Criteria

• Subjects with another form of ICI ie Netherton syndrome, Kid syndrome etc.
• Infectious/Immune-related Exclusions
• Medical History and Concurrent Diseases

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: SINGLE_GROUP

Arm && Interventions

Group	Intervention	Description
deucravacitinib treatment	deucravacitinib	challenge-dechallenge -rechallenge design

Primary Outcome Measures

Name	Time	Method
efficacy of deucravacitinib	week 44	number of new blister conting every day

Secondary Outcome Measures

Name	Time	Method
Safety of deucravacitinib treatment	week 44	record of adverse events

Trial Locations

Locations (1)

CHU de Nice; 🇫🇷 Nice, Chu de Nice, France