Onycomycosis Clinical Trial
Official title:
A Randomized Study to Evaluate the Efficacy of Herbal Ingredients Combined With a Carrier System (Phytonail) Compared With Amorolfine 5% Nail Lacquer (Loceryl) in the Treatment of Toenail Onychomycosis
Background: Onychomycosis, the most common nail disorder, is a superficial fungal infection
affecting toenails more than fingernails. Onychomycosis can cause pain and discomfort and
has the potential to be a source of morbidity. Although oral antifungal agents achieve a
better complete cure rate for onychomycosis, many patients are worried about the side
effects and unwilling to take oral medications. Phytonail is a mixture of herbal active
ingredients including tea tree oil, lavender oil and Australian blue cypress oil with
BioEqual carrier system. A preliminary trial has shown a 100% KOH negative rate in 32 nails
after 12 weeks of Phytonail therapy. Amorolfine 5% nail lacquer (Loceryl) is a
broad-spectrum morpholine antifungal demonstrated 60-75% mycological cure rate in several
randomized controlled trials for the treatment of toenail onychomycosis.
Objective: To evaluate the efficacy and safety of Phytonail relative to amorolfine 5% nail
lacquer in the treatment of toenail onychomycosis.
Methods: This is a randomized, parallel-group, open-labeled study in adult subjects with
toenail onychomycosis. In this study, 60 eligible patients will be randomized in a 1: 1
ratio to one of the two treatment groups: Phytonail or amorolfine 5% nail lacquer. Before
randomization, patients are to have onychomycosis in at least one great toenail with
positive KOH examination and positive fungal culture. During the treatment phase, Phytonail
will be applied twice daily and amorolfine 5% nail lacquer once weekly for 16 weeks to all
affected toenails. Physician's assessments and photographic analyses will be carried out at
baseline, Week 4, 8, 16, and 24. Mycological evaluation including KOH examination will be
performed at baseline, Week 4, 8, and 16. Fungal culture will be performed at baseline and
for KOH negative patients.
Subjects aged 20-65 years with toenail onychomychosis involved at least one great toenail
will be recruited in the study. Approximately 200 subjects will be screened, in order to
randomize 72 eligible subjects. Allowing for approximately 20% drop-outs, it is estimated
that for completing 60 eligible subjects, approximately 72 subjects would be enrolled.
Subjects must meet all the inclusion criteria and none of the exclusion criteria to receive
treatment assignment.
Procedures:
Explain study and obtain written informed consent: Screening Review inclusion/exclusion
criteria including prior and concomitant medications: Screening and Baseline (Day 1)
Demographics: Screening Medical history (including prior onychomycosis): Screening Personal
and family history as well as history of any prior treatment for onychomycosis and any
symptoms attributed to onychomycosis Physical examination: Screening Selection of target
great toenail: Screening Proper nail trimming of target great toenail (as needed): all
visits The subject's target great toenail will be properly trimmed as needed by the
investigator or a qualified designee. Proper nail trimming is defined as cutting the nail
plate to within 1 mm of the hyponychium or distal groove. In case of onycholysis the nail is
to be trimmed not to the proximal limit of the onycholysis.
Percentage of nail involvement of the target great toenail based on signs of onychomycosis:
all visits The percentage of involvement of the target great toenail will be determined by
the investigator's visual estimate of the extent of the total nail area that shows signs of
onychomycosis after proper trimming the nail.
Assessment of other toenails: all visits (except screening) At baseline (Day 1) and all
subsequent visits, the investigator will identify all other toenails (excluding the target
great toenail) with signs of onychomycosis and determine the total number of toenails that
are completely clear (0% involvement) or almost clear (<10% involvement).
Marking the target great toenail: all visits The investigator will ink the distal groove,
the 2-mm notch (except at Screening, when the notch will not have been made yet), and the
healthy/involved limit of the target toenail with a supplied indelible marking pen. These
markings on the target great toenail will be used to determine the CN, and will be used for
the calculation of CNG and LNG. The initial photo of the unmarked nail must be taken before
any marking is made.
Two-millimeter notch for the target great toenail: Baseline (Day 1) At the Baseline (Day 1)
visit, the investigator will make a superficial notch in the nail plate, approximately 2 mm
distal from the proximal nail fold. The investigator will ink the notch with a marking pen
at this and each subsequent visit. If, as the nail grows, the investigator feels that the
original notch may be clipped off at the next visit, a new nail notch approximately 2 mm
from the proximal nail fold will be made.
KOH examination of the target great toenail: Screening, Week 4, 8, and 16. Fungal culture of
the target great toenail: Screening, at Week 4, 8, and 16 only for KOH negative patients
Digital photography: Baseline (Day 1); Week 4, 8, 16, and 24; early termination (if
applicable)
Digital photographs will be analyzed for the following measurements:
Clear nail (CN) of the target great toenail: CN is defined as the distance (mm) between the
PNF and the most proximal limit of the disease (as marked by the investigator).
Clear nail growth (CNG) of the target great toenail: The CNG is a calculation and is defined
as the difference (mm) between the CN at a given visit and the CN at Baseline (Day 1). For
example, if the baseline CN is 2 mm and the Week 12 CN is 5 mm, the nail will have 3 mm of
new clear nail growth.
Linear nail growth (LNG) of the target great toenail: The LNG represents the growth of nail
plate (normal and mycotic) over a period of time. LNG is defined as the distance at any
given time point from the PNF to the nail notch, minus the distance of the notch from the
PNF at Baseline (2 mm). For example, if at a post-Baseline visit the length from the
proximal nail fold to the inked notch becomes 6 mm, then the nail will have growth 4 mm (6
mm- 2 mm= 4 mm).
Randomization: Baseline (Day 1) Subject dosing diary dispensing: Baseline (Day 1) through
Week 8 Subject dosing diary collection: Week 4 through Week 16, and early termination Study
drug dispensing: Baseline (Day 1) through Week 8 Study drug self-administration: Baseline
(Day 1) through Week 16 Study drug collection: Week 4 through Week 16, and early termination
Prior and concomitant drugs: All visits Record adverse events: All visits (except screening)
;
Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment