Mode
Text Size
Log in / Sign up
Phase 4 N=62 Treatment

Safety and Pharmacokinetics of Efinaconazole Topical Solution in Subjects With Mild to Severe Onychomycosis

Onychomycosis

Enrolled (actual)
62
Serious AEs
3.3%
Results posted
Nov 2021
Primary outcome: Primary: Percentage of Participants With at Least One Adverse Event — 39 Participants

Study Design & Population

Study type
Interventional
Phase
Phase 4
Interventions
Efinaconazole (Drug)
Age
Pediatric · 6+ yrs
Sex
All
Sponsor
Bausch Health Americas, Inc.
Primary completion
Jan 2019

Outcome Measures

OutcomeResultp-value
PRIMARY
Percentage of Participants With at Least One Adverse Event
39

Summary

Safety and Pharmacokinetics (PK) of a once daily topical application of efinaconazole in the treatment of pediatric subjects with mild to severe onychomycosis of the toenails.

Eligibility Criteria

Key Inclusion Criteria

  • Male or female subjects of any race, 6 to 16 years of age (inclusive). PK Subset: Male or female subjects of any race, 12 to 16 years of age (inclusive).
  • Verbal and written informed consent/assent obtained from the subject and/or their parent or legal guardian.
  • Good general health, as assessed by the investigator, based on the subject's medical history, physical examination, and safety laboratory tests.
  • Target great toenail for all subjects, and both great toenails for subjects in the PK subset, must have evidence of toenail growth, per subject's report that monthly clipping is needed.
  • Subjects and their parents/legal guardians are willing to comply with study instructions and return to the investigational center for all required visits (a visit schedule with the length of each visit will be provided to ensure that the subject can meet the requirements and have adequate transportation).

Key Exclusion Criteria

  • Females who are pregnant, nursing an infant, or planning a pregnancy during the study period.
  • History of immunosuppression and/or clinical signs indicative of possible immunosuppression, as determined by the investigator, or known human immunodeficiency virus infection.
  • History of diabetes that is uncontrolled as determined by the investigator (diabetes that is controlled by diet or medication does not exclude a subject).
  • Presence of any toenail infection other than or in addition to dermatophytes, such as Scytalidium as determined by the investigator (candidal onychomycosis infection, concurrent with a positive dermatophyte culture, is acceptable).
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT02812771). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

Back to search