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Netherton Syndrome clinical trials

View clinical trials related to Netherton Syndrome.

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NCT ID: NCT06137157 Recruiting - Netherton Syndrome Clinical Trials

Evaluation of Topical ATR12-351 in Adults With Netherton Syndrome

Start date: June 19, 2024
Phase: Phase 1
Study type: Interventional

The objectives of this clinical trial are to evaluate the safety and tolerability of topically applied ATR12-351, to understand what the body does to ATR12-351, and to observe treatment benefits of the drug in approximately 12 adult patients with Netherton Syndrome (NS). ATR12-351 will be applied to skin lesions on one side of the body, while the vehicle control will be applied to similar lesion on the other side of the body twice daily for 2 weeks.

NCT ID: NCT05979831 Recruiting - Netherton Syndrome Clinical Trials

A Study to Explore Safety, Pharmacokinetics, and Early Clinical Signal of Efficacy of DS-2325a in Patients With Netherton Syndrome

Start date: September 28, 2023
Phase: Phase 1/Phase 2
Study type: Interventional

Netherton Syndrome (NS) is a severe rare disease characterized by generalized scaling, erythema, and epidermal barrier defects. This study assessed the safety, pharmacokinetics (PK), and efficacy of DS-2325a in patients with NS.

NCT ID: NCT05902663 Not yet recruiting - Netherton Syndrome Clinical Trials

Natural History of Netherton Syndrome

Start date: June 18, 2024
Phase:
Study type: Observational

The goal of this non-interventional study (NIS) is to collect real-world data to describe the natural history of Netherton Syndrome (NS).

NCT ID: NCT05856526 Recruiting - Netherton Syndrome Clinical Trials

A Study to Test Whether Spesolimab Helps People With a Skin Disease Called Netherton Syndrome

Start date: May 15, 2023
Phase: Phase 2/Phase 3
Study type: Interventional

This study is open to people with a skin disease called Netherton syndrome (NS). People can join the study if they are 12 years and older. The purpose of this study is to find out whether a medicine called spesolimab helps people with NS. Participants are divided into a spesolimab and a placebo group. Placebo injections look like spesolimab injections but do not contain any medicine. Every participant has a 2 in 3 chance of being in the spesolimab group. In the beginning, participants get the study medicine as an injection into a vein. Afterwards, they get it as an injection under the skin every month. After 4 months, participants in the placebo group switch to spesolimab treatment. Participants are in the study for about 1 year. During this time, they visit the study site 16 times. Where possible, 4 of 16 visits can be done at the participant's home instead of the study site. The doctors regularly check participants' NS symptoms. The results are compared between the groups to see whether spesolimab works. The doctors also regularly check participants' general health and take note of any unwanted effects.

NCT ID: NCT05789056 Recruiting - Netherton Syndrome Clinical Trials

Open Label, Safety and Efficacy Study of QRX003 Lotion in Subjects With Netherton Syndrome

Start date: March 14, 2023
Phase: Phase 2/Phase 3
Study type: Interventional

To assess the safety, tolerability, and efficacy of QRX003 lotion (4%) when added to standard of care treatment regimen, including systemic therapy in subjects with Netherton syndrome

NCT ID: NCT05583669 Completed - Netherton Syndrome Clinical Trials

A Study to Assess the Safety and Pharmacokinetics of Multiple Ascending Subcutaneous Doses of DS-2325a in Healthy Subjects

Start date: November 8, 2022
Phase: Phase 1
Study type: Interventional

Netherton syndrome (NS) is a rare autosomal recessive disease and no systemic treatment or standard of care currently exists for patients with NS. DS-2325a, a specific and potent inhibitor of kallikrein 5, is expected to treat NS by replacing a defective gene.

NCT ID: NCT05521438 Recruiting - Netherton Syndrome Clinical Trials

Safety, Tolerability and Efficacy of QRX003 Lotion in Subjects With Netherton Syndrome

Start date: June 23, 2022
Phase: Phase 2/Phase 3
Study type: Interventional

This study has been designed to determine the safety, tolerability and efficacy of QRX003 lotion 2%, 4% QAM or 4% BID in subjects with Netherton Syndrome (NS) in comparison to vehicle

NCT ID: NCT05388903 Completed - Netherton Syndrome Clinical Trials

A Study to Assess the Safety and Pharmacokinetics of Single Ascending Subcutaneous and Intravenous Doses of DS-2325a in Healthy Subjects

Start date: June 20, 2022
Phase: Phase 1
Study type: Interventional

Netherton syndrome (NS) is a rare autosomal recessive disease and no systemic treatment or standard of care currently exists for patients with NS. DS-2325a, a specific and potent inhibitor of kallikrein 5, is expected to treat NS by replacing a defective gene.

NCT ID: NCT05211830 Recruiting - Netherton Syndrome Clinical Trials

A Study to Evaluate Topically Applied SXR1096 Cream in Patients With Netherton Syndrome

Start date: December 7, 2021
Phase: Phase 1/Phase 2
Study type: Interventional

In this phase I/II trial a topical skin cream with the active substance SXR1096 will be tested in patients with Netherton syndroms, a rare inflammatory skin disease. SXR1096 is a specific and potent protease inhibitor that can inhibit the proteases kallikrein 5, 7 and 14 - all recognised as up-regulated and causing the disease state in Netherton syndrome patients. Patients will be treated for one month with active cream and placebo cream at different areas of the skin.

NCT ID: NCT04244006 Recruiting - Netherton Syndrome Clinical Trials

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

NS-DUPI
Start date: July 23, 2020
Phase: Phase 2/Phase 3
Study type: Interventional

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.