A Pilot Study of the Efficacy and Safety of Dupilumab Versus Placebo in Patients With Netherton Syndrome

NCT ID: NCT04244006

Last Updated: 2023-08-23

Basic Information

• Recruitment Status: UNKNOWN
• Clinical Phase: PHASE2/PHASE3
• Total Enrollment: 24 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2020-07-23
• Study Completion Date: 2024-06-01

Brief Summary

To date, there are no effective therapy for the management of Netherton Syndrome (NS) Patients use emollients with a limited efficacy on scaling and no efficacy on skin inflammation and pruritus. They may also use topical corticosteroids or calcineurin inhibitors in case of eczematous lesions. The use of therapies targeting skin inflammation has been reported in a few case reports. Their efficacy is very limited and their uses are limited because of the chronicity of the disease, the impaired skin barrier function and the risk for skin infections and skin cancers. Therefore, there is a huge medical need for novel therapies in NS.The expected consequences of this study are that a 16-week course of dupilumab will be more effective than placebo for the treatment of moderate to severe NS Dupilumab could therefore improve skin condition and quality of life.

Detailed Description

This is a proof of concept (pilot) double-blind randomized placebo-controlled study evaluating the efficacy and safety of dupilumab for the treatment of NS. Patients will be randomized in a 2:1 ratio to receive dupilumab (2 doses of 300 mg), or placebo, at baseline and then 1 dose of dupilumab 300 mg, or placebo, every 2 weeks until week 14 (total of 8 administrations).Moderate to severe NS were selected in order to be able to measure the improvement of skin condition.

Conditions

Netherton Syndrome

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: TREATMENT
• Blinding Strategy: TRIPLE

Study Groups

Dupilumab

The patient will receive 2 doses at baseline and then 1 dose every 2 weeks (8 administrations in total) of Dupilumab 300 mg (syringe of 2 mL for subcutaneous administration).

Group Type: EXPERIMENTAL

Dupilumab Prefilled Syringe

Intervention Type: DRUG

administration of dupilumab corresponding to dupilumab arm

Placebo

The patient will receive 2 doses at baseline and then 1 dose every 2 weeks (8 administrations in total) of placebo (syringe of 2 mL for subcutaneous administration)..

Group Type: PLACEBO_COMPARATOR

Placebo Prefilled Syringe

Intervention Type: OTHER

administration of placebo corresponding to placebo arm

Interventions

Dupilumab Prefilled Syringe

administration of dupilumab corresponding to dupilumab arm

Intervention Type: DRUG

Placebo Prefilled Syringe

administration of placebo corresponding to placebo arm

Intervention Type: OTHER

Eligibility Criteria

Inclusion Criteria

• Adult patients affiliated to a social insurance protection regimen.
• Clinical diagnosis of NS (7) (trichorrhexis invaginata, extensive scaling, skin inflammation, allergic manifestations) and absent or marked reduction of LEKTI staining.
• Moderate to severe forms: NASA (Netherton Area Severity Assessment score) score ≥ 5/12 at inclusion.
• Patients able to understand the study procedures including the ability to complete patient-based self-assessment questionnaires.
• Patients who agree to sign the written informed consent.

Exclusion Criteria

• Hypersensitivity to dupilumab or its excipients.
• Modification of the usual treatment (emollients and topical corticosteroids used on a regular basis) within 2 weeks before inclusion.
• Treatment with topical calcineurin inhibitors 1 week before inclusion.
• Treatment with oral immunosuppressant (including cyclosporine, methotrexate, azathioprine, mycophenolate mofetil), oral retinoids (acitretin, alitretinoin, isotretinoin) or phototherapy within 4 weeks before inclusion.
• Treatment with immunomodulating biologics (Tumor Necrosis Factor (TNF) inhibitor) 16 weeks before inclusion.
• Treatment with another investigational drug within 8 weeks before inclusion.
• Treatment with a systemic antibiotic within 2 weeks before inclusion.
• Active skin infection requiring the use of a systemic therapy within 2 weeks before the inclusion.
• Any other condition that according to the investigator will impair the ability to evaluate treatment effect.
• Known or suspected history of immunosuppression, including history of invasive opportunistic infections (e.g., tuberculosis, histoplasmosis, listeriosis, coccidioidomycosis, pneumocystis, aspergillosis).
• Current infections including infection with helminthes.
• Pregnant or breastfeeding women, or women planning to become pregnant or breastfeed during the study. Women of childbearing age, potentially sexually active, and unwilling to use adequate birth control methods.
• Mental or physical incapacity to fill in the questionnaires.

• Minimum Eligible Age: 18 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

MedSharing

UNKNOWN

Sponsor Role: collaborator

University Hospital, Toulouse

OTHER

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Juliette MAZEREEUW-HAUTIER

Role: PRINCIPAL_INVESTIGATOR

Toulouse Hospital

Locations

Dermatologie Necker

Paris, , France

Site Status: NOT_YET_RECRUITING

Dermatology

Toulouse, , France

Site Status: RECRUITING

Countries

France

Central Contacts

Nadège ALGANS

Role: CONTACT

algans.n@chu-toulouse.fr

0561777204 ext. +33

Helene TEXIER

Role: CONTACT

texier.h@chu-toulouse.fr

Facility Contacts

tobecompleted

Role: primary

Helene TEXIER

Role: primary

texier.h@chu-toulouse.fr

Other Identifiers

RC31/19/0045

Identifier Type: -

Identifier Source: org_study_id