A Randomized Double-blinded Pilot Study of the Efficacy and Safety of Dupilumab Versus Placebo in Patients With Netherton Syndrome
试验速览
- 阶段
- 2 期
- 状态
- 招募中
- 入组人数
- 24
- 试验地点
- 2
- 主要终点
- The severity of the disease of the Netherton Area Severity Assessment score (NASA).
研究概览
简要总结
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.
详细描述
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.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Parallel
- 主要目的
- Treatment
- 盲法
- Triple (Participant, Care Provider, Investigator)
盲法说明
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.
入排标准
- 年龄范围
- 18 Years 至 —（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •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.
排除标准
- •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.
研究组 & 干预措施
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).
干预措施: Dupilumab Prefilled Syringe (Drug)
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)..
干预措施: Placebo Prefilled Syringe (Other)
结局指标
主要结局
The severity of the disease of the Netherton Area Severity Assessment score (NASA).
时间窗: Day 0 and week 16
NASA score
次要结局
- 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)
- 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)
- QOL score(Day 0, Week 16 and 28)
- Microbiome qualitative and quantitative analysis(Day 0 and week 16)
- Safety of dupilumab(Day 0, week 2, week 4, week 6, week 8, week 10, week 12, week 14, week 16, week 28)
- 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)
- Skin inflammation(Day 0 and week 16)
- Protease activity(Day 0 and week 16)
- Transepidermal water loss (TEWL)(Day 0 and Week 16)