Topically Applied AMTX-100 CF for Adult Patients With Mild to Moderate Atopic Dermatitis

Completed · Phase 1/Phase 2 · Has a placebo group

Conditions studied: Atopic Dermatitis

In brief

This study determines the Maximum Tolerable Dose (MTD) by maximum BSA percentage treated and evaluates safety and efficacy of 1.1% w/w AMTX-100 CF versus placebo (vehicle). The study has two parts: Phase I (Part 1): Approximately Twenty-five (25) subjects with various treatable Body Surface Area (BSA) involvement of Mild to Moderate Atopic Dermatitis will be enrolled in the study and treated with 1.1% w/w AMTX-100 CF. Phase II (Part 2): Approximately sixty (60) subjects with Mild to Moderate Atopic Dermatitis with various treatable BSA involvement of Mild to Moderate Atopic Dermatitis will be randomized to be treated with 1.1% w/w AMTX-100 CF3 concentration or Vehicle (Placebo) in the study.

Key facts

Study ID
NCT04313400
Run by
Amytrx Therapeutics, Inc.
People needed
91
Starts
2020-03-10
Expected to finish
2024-01-02
Last updated by the study team
2025-05-02

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

Where it is running

Full record on ClinicalTrials.gov

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