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Evaluation of Topical ATR12-351 in Adults with Netherton Syndrome

Phase 1
Recruiting
Conditions
Netherton Syndrome
Interventions
Registration Number
NCT06137157
Lead Sponsor
Azitra Inc.
Brief Summary

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.

Detailed Description

Netherton syndrome (NS) is a rare but severe autosomal recessive disease that affects the skin, hair, and immune system. NS presents at birth with red skin covered by fine scales, a specific hair shaft abnormality ("bamboo hair"), atopic lesions, and elevated systemic immunoglobulin E (IgE) levels. Patients often develop allergies and asthma, and the unfortunate prognosis for infants with NS is poor, with 10% mortality in the first 6 months of life and recurrent infections. There are no FDA-approved treatment options for NS. NS is caused by mutations in in the SPINK5 gene encoding the serine protease inhibitor lymphoepithelial Kazal-type related inhibitor (LEKTI). Absence of LEKTI causes unregulated activity of proteases in the kallikrein subfamily, causing excessive desquamation of skin.

ATR12-351 is a topical ointment containing a lyophilized version of a live biotherapeutic product (LBP), Staphylococcus epidermidis (SE) strain designated SE351. This strain has been modified to be auxotrophic and to express recombinant human LEKTI protein (rhLEKTI). ATR12-351 is intended to address the underlying cause of NS by replacing deficient/dysfunctional LEKTI. The treatment consists of applying ATR12-351 to affected areas, where rhLEKTI produced by ATR12-351 will counter the dysregulated skin serine protease activity observed in NS patients.

This first-in-human study is a randomized, double-blind, vehicle-controlled clinical study to assess the safety, tolerability, and pharmacokinetics (PK) of topical ATR12-351 in approximately 12 adult Netherton syndrome patients who will serve as their own control. This study will include a 14-day treatment period to investigate the safety and tolerability of ATR12-351 applied to the skin and will be followed a total of 84 days for safety. The results of this first-in-human clinical study will establish safety and tolerability as well as initial efficacy of ATR12-351 application in Netherton syndrome patients.

Recruitment & Eligibility

Status
RECRUITING
Sex
All
Target Recruitment
12
Inclusion Criteria
  • Adults ≥18 years of age
  • Confirmed mutation of the serine protease inhibitor of Kazal type 5 (SPINK5) gene
  • Involvement of ≥20% of body surface area with skin changes consistent with Netherton syndrome
Exclusion Criteria
  • Use of biologic therapies, antibiotics, antihistamines, corticosteroids, retinoids, disease-modifying antirheumatic drugs (DMARDs), immunosuppressive agents, phosphodiesterase-4 (PDE4) inhibitors, topical calcineurin inhibitors, or topical Janus kinase (JAK) inhibitors
  • Open wounds or extensive areas of excoriation precluding identification of appropriate application sites in the Investigator's judgment
  • Concurrent involvement in any other clinical study/expanded access program with an investigational drug or device or has participated in a clinical study within 30 days prior to the screening visit
  • Residing with an immunocompromised person in the same dwelling from the baseline visit through 2 weeks after the treatment period
  • History of ultraviolet phototherapy within the planned treatment area 4 weeks prior to baseline

Study & Design

Study Type
INTERVENTIONAL
Study Design
SINGLE_GROUP
Arm && Interventions
GroupInterventionDescription
Internal controlled armATR12-351ATR12-351 on left side of body, vehicle on right side of body in one group; vehicle on left side of body, ATR12-351 on right side of body.
Primary Outcome Measures
NameTimeMethod
Adverse events84 days

Incidence, severity, seriousness and relatedness of all treatment-emergent adverse events

Secondary Outcome Measures
NameTimeMethod
Pharmacokinetics: skin concentration (Cmax skin)42 days

Concentration of rhLEKTI in the skin (pmol/cm2), measured by tape stripping, following topical application.

Investigator's Global Assessment (IGA)42 days

Visual assessment of the overall severity of skin disease severity at each application site, using a 5-point scale (0, clear; 1, almost clear/minimal; 2, mild; 3, moderate; 4, severe). Higher scores indicate greater severity.

Pharmacokinetics: plasma concentration42 days

Concentration (ng/mL) of rhLEKTI in the plasma following topical application.

Patient's Global Assessment (PGA)42 days

Visual assessment of the overall severity of skin disease severity at each application site, using a 5-point scale (0, clear; 1, almost clear/minimal; 2, mild; 3, moderate; 4, severe). Higher scores indicate greater severity.

NS-modified SCORAD42 days

The investigator's objective assessment of the severity (peeling, scaling, lichenification, erythema, papules) and extent (surface of affected skin areas) of skin disease at each application site is combined with patient's subjective scores (pain and pruritus). Higher scores indicate greater severity with a maximum of 100 points possible.

Trial Locations

Locations (2)

Stanford University

🇺🇸

Palo Alto, California, United States

Yale University

🇺🇸

New Haven, Connecticut, United States

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