A Study of ATB1651 in Adults With Mild to Moderate Onychomycosis

PHASE1CompletedINTERVENTIONAL
Enrollment

30

Participants

Timeline

Start Date

March 4, 2022

Primary Completion Date

June 3, 2023

Study Completion Date

September 20, 2023

Conditions
Onychomycosis
Interventions
DRUG

ATB1651, 2 mg/mL

The participants will apply daily doses of ATB1651, 2 mg/mL to all 10 toenails including at least 1 affected great toenail for 28 days

DRUG

ATB1651, 5 mg/mL

The participants will apply daily doses of ATB1651, 5 mg/mL to all 10 toenails including at least 1 affected great toenail for 28 days

DRUG

ATB1651, 10 mg/mL

The participants will apply daily doses of ATB1651, 10 mg/mL to all 10 toenails including at least 1 affected great toenail for 28 days

DRUG

ATB1651, 20 mg/mL

The participants will apply daily doses of ATB1651, 20 mg/mL to all 10 toenails including at least 1 affected great toenail for 28 days

DRUG

ATB1651, 30 mg/mL

The participants will apply daily doses of ATB1651, 30 mg/mL to all 10 toenails including at least 1 affected great toenail for 28 days

OTHER

Placebo

The participants will apply placebo to all 10 toenails including at least 1 affected great toenail for 28 days

Trial Locations (1)

8011

New Zealand Clinical Research Christchurch, Christchurch

All Listed Sponsors
collaborator

Novotech (Australia) Pty Limited

INDUSTRY

lead

AmtixBio Co., Ltd.

INDUSTRY