Study to Evaluate the Efficacy and Safety of P-3058 Nail Solution in the Treatment of Onychomycosis

Withdrawn before enrolling · Phase 3

Conditions studied: Onychomycosis of Toenail

In brief

The aim of this phase III study is to establish the efficacy and safety of P-3058 (terbinafine 10% nail solution) topically administered once weekly in patients with onychomycosis in comparison to the Vehicle in a double-blind fashion. The overall treatment period will be of 48 weeks.

Key facts

Study ID

NCT03094468

Run by

Polichem S.A.

People needed

0

Starts

2017-05-01

Expected to finish

2019-12-01

Last updated by the study team

2018-01-10

Who can join

Age: 12 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Written informed consent before starting any study related procedures.
• Patients aged 12 and older of any race.
• Males or females.
• Outpatients.
• Clinically diagnosed mild-to-moderate distal lateral subungual onychomycosis (DLSO) of at least one great toenail (the "target nail") at the Screening visit (V1).
• Patients with onychomycosis involving ≥ 20% to ≤ 50% of the area of the target great toenail.
• Patients with a positive KOH examination.
• Patients with positive culture for dermatophyte(s).
• Evidence of target great toenail growth reported by the patient defined as at least monthly nail clipping.

You may not qualify if…

• Woman who is pregnant, nursing an infant, or planning a pregnancy during the study period.
• Patients with history of allergic reactions to terbinafine or its excipients.
• Use of any investigational drug/device or participation in a previous clinical trial within four weeks prior to Screening visit (V1).
• Patients using nail polish or other nail cosmetic product on the concerned nails from at least 24 hours prior to Screening visit (V1) until the end of the study.
• Use of systemic antifungal drugs in the 24 weeks prior to Screening visit (V1) or non-responsive to systemic antifungal therapy for onychomycosis.
• Nail application of topical antifungal drugs or device in the 4 weeks prior to Screening visit (V1).
• Presence of any nail infections other than dermatophyte.
• Presence of onychodystrophy that could interfere with clinical assessments.
• Presence of "yellow spikes" on the target nail.
• Presence of dermatophytoma on the target nail.
• Presence of nail thickness exceeding 2 mm.
• Patients with proximal subungual involvement (marker of immunosuppressed patient).
• Patients with severe plantar or moccasin tinea pedis (defined by blistering, pustules or inability to ambulate).
• Patients with nail abnormalities due to conditions like psoriasis, lichen planus, immune dysfunction, collagen-vascular diseases, peripheral vascular disease.
• Patients with life expectancy less than 2 years.
• Chemotherapy, immunosuppressive therapy in the 12 weeks prior to Screening visit (V1).
• Systemic corticosteroids, antimetabolites and immune-stimulants therapy in the 4 weeks prior to Screening visit (V1).
• HIV infection or any other immunodeficiency.
• Alcohol or substance abuse.
• Patients/parents (or legal guardian) unable to understand the procedures and purposes of the study.
• Any other condition that, in the opinion of the Investigator, would prevent the subject from effectively participating in the study, place the subject at risk or effect the assessment of efficacy and safety of the study medication.

Where it is running

• Polichem Investigation Site no 45 — North Hollywood, California, United States
• Polichem Investigation Site no 5 — Oceanside, California, United States
• Polichem Investigation Site no 39 — San Diego, California, United States
• Polichem Investigation Site no 2 — Hialeah, Florida, United States
• Polichem Investigation Site no 23 — Jacksonville, Florida, United States
• Polichem Investigation Site no 22 — Miami, Florida, United States
• Polichem Investigation Site no 52 — Louisville, Kentucky, United States
• Polichem Investigation Site no 41 — Portsmouth, New Hampshire, United States
• Polichem Investigation site no 1 — New York, New York, United States
• Polichem Investigation Site no 44 — Cincinnati, Ohio, United States
• Polichem Investigation Site no 40 — Norman, Oklahoma, United States
• Polichem Investigation Site no 14 — Oklahoma City, Oklahoma, United States
• Polichem Investigation Site no 10 — Austin, Texas, United States
• Polichem Investigation Site no 11 — Dallas, Texas, United States
• Polichem Investigation Site no 43 — Dallas, Texas, United States
• Polichem Investigation Site no 6 — Fort Worth, Texas, United States
• Polichem Investigation Site no 12 — Houston, Texas, United States
• Polichem Investigation Site no 4 — Houston, Texas, United States
• Polichem Investigation Site no 42 — Pflugerville, Texas, United States
• Polichem Investigation Site no 53 — San Antonio, Texas, United States
• Polichem Investigation Site no 54 — San Antonio, Texas, United States
• Polichem Investigation site no 3 — Calgary, Alberta, Canada
• Polichem Investigation Site no 8 — Edmonton, Alberta, Canada
• Polichem Investigation Site no 13 — Mississauga, Ontario, Canada
• Polichem Investigation Site no 9 — Richmond Hill, Ontario, Canada

Full record on ClinicalTrials.gov

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