Safety and PK Study of Ha44 Gel Under Maximal Use Conditions for Treatment of Head Lice Infestation

Phase 2

Completed

Brief Summary: The purpose of the study is to evaluate the safety and tolerability of a single application of Ha44 Gel 0.74% w/v for the treatment of head lice under maximal use conditions.

Secondary objective is to evaluate pharmacokinetics of Ha44 and benzyl alcohol (contained in Ha44 vehicle) under maximal use conditions.

Detailed Description: This is an open-label safety and pharmacokinetic (PK) study involving a single application of Ha44 Gel 0.74% administered under maximal use conditions.

All participants must have an active head lice infestation (at least 3 live lice) and be 6 months to 17 years of age. The study will enroll approximately 36 pediatric subjects between the ages of 6 months and 17 years.

Pediatric PK samples will be collected at 0 (predose), 30 and 60 mins and 2 and 8 hrs time points.

More than one household member with an active lice infestation may participate in the study. Eligible subjects will be consented and screened for study eligibility on Day 0 (Visit 1). All subjects will return to the study site for three follow-up clinic visits at Days 1, 7 and 14. The maximum study duration for a subject is 16 days.

Recruitment & Eligibility

Inclusion Criteria

Male or female
6 months to 17 years of age
Be in good health, as determined by medical history and physical examination
Has an active head lice infestation at screening as determined by an experienced evaluator. An active infestation is defined as the presence of at least 3 live lice.
Female subjects must be:
- Of non-childbearing potential (no history of menstrual periods, post-hysterectomy, or post-menopausal for at least 2 years) OR,
- If of childbearing potential, must have a negative urine pregnancy test prior to treatment and agree to use a highly effective method of contraception from Day 0 through the Day 14 visit. Acceptable methods of contraception include abstinence, vasectomized partner, tubal ligation, combined oral hormonal contraceptive, contraceptive injection, contraceptive patch, or IUD. If a hormonal contraception is the only method, the subject must have been on a stable dose for at least 3 months.
The parent/guardian agrees to allow serial blood samples collected from subject for PK analysis during study.
Has signed an informed consent and/or assent form (ICF).

Exclusion Criteria

Has a condition or illness that, in the opinion of the Investigator, may interfere with the study results.
Has current dermatological disease or inflammation on the face, scalp, ears, neck or back, including eczema, atopic dermatitis, alopecia, psoriasis or any other chronic skin disease that, in the opinion of the Investigator, would interfere with the safety or PK evaluation.
Had a prior reaction to products containing piperonyl butoxide, pyrethrin, or pyrethrum extract.
Has been using hormonal contraception for less than 3 months.
Is pregnant or currently nursing.
Receiving systemic or topical medication, which in the opinion of the Investigator, may interfere with the study results.
Has received an investigational agent within 30 days prior to Day 0.

Arm && Interventions

Group	Intervention	Description
1	Ha44 Gel	Ha44 Gel 0.74%, topical solution, maximum feasible amount applied for 10 minutes

Primary Outcome Measures

Name	Time	Method
Number of the Subjects With AEs.	3 months	Safety and tolerability assessed by AEs. Number of subjects with reporting AEs.

Secondary Outcome Measures

Name	Time	Method
Pk Parameters: Cmax	0 to 8 hours	Maximum concentration of Ha44 (Cmax)
PK Parameters: Tmax	0-8 hours	Time to maximum concentration of Ha44 (Tmax)
PK Parameters: AUC(0-8)	0-8 hours	Area under the concentration-time curve of Ha44 (AUC 0-8)