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Evaluation of Topical ATR12-351 in Adults With Netherton Syndrome
Sponsor: Azitra Inc.
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.
Official title: A Randomized, Double-Blind, Vehicle-Controlled, First-in-Human Safety, Tolerability and Proof-of-Concept Study of Topical ATR12-351 in Adults With Netherton Syndrome
Key Details
Gender
All
Age Range
18 Years - Any
Study Type
INTERVENTIONAL
Enrollment
12
Start Date
2024-06-19
Completion Date
2026-08-01
Last Updated
2026-02-05
Healthy Volunteers
No
Conditions
Interventions
ATR12-351
Topical ointment containing ATR12-351, a LEKTI-secreting strain of S. epidermidis
Locations (2)
Stanford University
Palo Alto, California, United States
Yale University
New Haven, Connecticut, United States