Phase 2 study to assess the safety and effectiveness of a product to treat children and adults with head lice
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
QUADRUPLE
Enrollment
142
Low Dose Ha44 Gel applied to scalp and hair for 10 minutes
High Dose Ha44 Gel applied to scalp and hair for 10 minutes
Placebo- vehicle Ha44 Gel without active ingredient applied to scalp and hair for 10 minutes
Universal BioPharma Research Institute, Inc.
Dinuba, California, United States
Axis Clinical Trials
Los Angeles, California, United States
Number of Participants Who Are Lice Free at All Follow-up Visits (Day 1, 7 and 14) Through the Day 14 Visit
Time frame: Follow up visit at days 1, 7 and 14 days
Safety and Tolerability of Ha44 Gel
The number of subjects with Treatment emergent AEs (TEAEs) related to the study medication will be reported by treatment group.
Time frame: From treatment to last visit of the study at 14 days
This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.