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RECRUITING
NCT06137157
PHASE1

Evaluation of Topical ATR12-351 in Adults With Netherton Syndrome

Sponsor: Azitra Inc.

View on ClinicalTrials.gov

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

Interventions

DRUG

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