Netherton Syndrome
Conditions
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.
Interventions
administration of dupilumab corresponding to dupilumab arm
OTHERPlacebo Prefilled Syringe
administration of placebo corresponding to placebo arm
Sponsors
MedSharing
University Hospital, Toulouse
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
TRIPLE (Subject, Caregiver, Investigator)
Masking description
Dupilumab and placebo will be provided in identically matching 2 mL pre-filled syringes. To protect the blind, each treatment kit of 2 mL (dupilumab/placebo) glass pre-filled syringes will be prepared such that the treatments (dupilumab and its matching placebo) are identical and indistinguishable and will be labeled with a treatment kit number.
Intervention model description
one arm with dupilumab (2/3 of patients) and one arm with placebo (1/3 of patients)
Eligibility
Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No
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.
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| The severity of the disease of the Netherton Area Severity Assessment score (NASA). | Day 0 and week 16 | NASA score |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Presence of infections (adverse event) | Day 0, week 2, week 4, week 6, week 8, week 10, week 12, week 14, week 16, week 28 | Number of Bacterial or viral Skin infections |
| Quantity of dermocorticosteroids used between each visit will be evaluated by questioning the patient. | Day 0, week 2, week 4, week 6, week 8, week 10, week 12, week 14, week 16, week 28 | number of tubes multiplied by the weight of one tube |
| QOL score | Day 0, Week 16 and 28 | QOL score |
| Skin inflammation | Day 0 and week 16 | number of inflammation markers on biopsies |
| Clinical efficacy severity of pruritus and pain | Day 0, week 2, week 4, week 6, week 8, week 10, week 12, week 14, week 16, week 28 | NASA score |
| Microbiome qualitative and quantitative analysis | Day 0 and week 16 | number and form of bacteria |
| Transepidermal water loss (TEWL) | Day 0 and Week 16 | Measured by a Tewameter applied on a standardized area in the anterior aspect of the forearm, |
| Safety of dupilumab | Day 0, week 2, week 4, week 6, week 8, week 10, week 12, week 14, week 16, week 28 | Blood tests performed every month until Week 16 (liver and renal tests, total blood count) |
| Protease activity | Day 0 and week 16 | number of protease markers on biopsies |
Countries
France
Contacts
Primary ContactNadège ALGANS
Backup ContactHelene TEXIER
Outcome results
None listed