PK and Safety Study of Natroba Topical Suspension 0.9% in Subjects 1 Month to 3 Years 11 Months of Age With Scabies

NCT ID: NCT05310734

Last Updated: 2025-02-14

Basic Information

• Recruitment Status: RECRUITING
• Clinical Phase: PHASE4
• Total Enrollment: 50 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2022-03-04
• Study Completion Date: 2026-03-31

Brief Summary

A population of approximately 50 pediatric subjects will be enrolled to assess the PK of spinosad and benzyl alcohol for 3 hours following a single, full-body topical application (open label) on a single in-clinic visit (Day 1, or Day 2 if screening only on Day 1). There will be approximately 50 subjects ages 1 month to 3 years 11 months of age enrolled with the goal of completing approximately 16 subjects. With assistance from a caregiver, Natroba will be applied over the entire body from the neck down to the toes (including the soles of the feet) and to the hairline, temples, forehead and possibly the scalp (if a scabies infestation is present on the scalp). The open-label Investigational Product (IP) will remain on the skin for at least 6 hours before removing the IP by gentle washing. The subjects will stay in the clinic until the 3-hour procedures are completed. Blood draws will be taken at 0 hours just prior to treatment, and then at 0.5 and 3.0 hours post-treatment. Heel sticks are likely to be the mode of blood collection for children less than 2 years of age. A ±5-minute time window will be allowed for all post-treatment blood samples. Removal of IP can occur by the caregiver at home after it has been on the skin for at least 6 hours before bathing the child. Safety will be assessed with adverse events (AEs), general skin and eye irritation assessments, and pre-dose and pre-discharge laboratory evaluations. Following the sample collections subjects will be released from the clinic and directed to their primary care physician for follow-up. Subjects will be provided scabies medications upon discharge to dispense to family members. These include 5% Permethrin for those in the household that are less than 4 years of age and Natroba for those in the household 4 years of age and older. Subjects who terminate early will not be given these medications to dispense to family members.

Detailed Description

A population of approximately 50 pediatric subjects will be enrolled to assess the PK of spinosad and benzyl alcohol for 3 hours following a single, full-body topical application (open label) on a single in-clinic visit (Day 1, or Day 2 if screening only on Day 1). There will be approximately 50 subjects ages 1 month to 3 years 11 months of age enrolled with the goal of completing approximately 16 subjects. With assistance from a caregiver, Natroba will be applied over the entire body from the neck down to the toes (including the soles of the feet) and to the hairline, temples, forehead and possibly the scalp (if a scabies infestation is present on the scalp). The open-label Investigational Product (IP) will remain on the skin for at least 6 hours before removing the IP by gentle washing. The subjects will stay in the clinic until the 3-hour procedures are completed. Blood draws will be taken at 0 hours just prior to treatment, and then at 0.5 and 3.0 hours post-treatment. Heel sticks are likely to be the mode of blood collection for children less than 2 years of age. A ±5-minute time window will be allowed for all post-treatment blood samples. Removal of IP can occur by the caregiver at home after it has been on the skin for at least 6 hours before bathing the child. Safety will be assessed with adverse events (AEs), general skin and eye irritation assessments, and pre-dose and pre-discharge laboratory evaluations. Following the sample collections subjects will be released from the clinic and directed to their primary care physician for follow-up. Subjects will be provided scabies medications upon discharge to dispense to family members. These include 5% Permethrin for those in the household that are less than 4 years of age and Natroba for those in the household 4 years of age and older. Subjects who terminate early will not be given these medications to dispense to family members.

Natroba (spinosad) Topical Suspension, 0.9% w/w applied by a parent/guardian in a single, full-body topical application from the neck down to the toes (including the soles of the feet) and to the hairline, temples, forehead and possibly the scalp (if a scabies infestation is present on the scalp).

A blood draw will be taken from subjects just before spinosad application (t=0) and then at 0.5 and3.0 hours. The following PK parameters will be calculated for spinosad (spinosyn A and spinosyn D) and benzyl alcohol in each subject: Cmax, Tmax, and Area Under the Curve (AUC) 0-12h.

Safety assessments include monitoring of AEs on study Day 1 or Day 2, general skin and eye irritation assessment on Day 1 or Day 2, laboratory assessments on Day 1 or Day 2, prior medications, and concomitant medications on Day 1 (and Day 2, if applicable). Smaller laboratory blood samples will be collected pre-dose and 12-hours post-dose prior to discharge.

Pharmacokinetic (PK) parameters will be calculated by using model independent methods. Standard statistical analyses will be done on these parameters for the purpose of interpretation of the data (Cmax, Tmax and Area Under the Curve (AUC) 0-3h and will be used to assess the absorption over 3 hours post-administration in 50 subjects (1 month - 3 years 11 months). The PK parameter estimates will be computed with noncompartmental methods for each subject. Individual elapsed sampling times (actual time) will be used in the PK analysis and parameters will be computed for each subject. Descriptive summaries of the plasma concentration levels for both spinosad (spinosyn A and spinosyn D) and benzyl alcohol observed at each nominal time point will be provided. Descriptive summaries of the PK parameter estimates will also be completed. Summary statistics for continuous variables will include number of non-missing observations, mean, standard deviation, coefficient of variation (CV%), median, minimum, and maximum, geometric mean and standard error of the geometric mean.

The safety endpoints include the evaluation of adverse events, general skin and eye irritation assessments, clinical laboratory assessments, and use of prior medications and concomitant medications. Additionally, the descriptive changes from baseline (pre-dose) to final assessment (pre-discharge) will be calculated for applicable parameters.

Conditions

Scabies

Study Design

• Allocation Method: NA
• Intervention Model: SINGLE_GROUP
• Primary Study Purpose: BASIC_SCIENCE
• Blinding Strategy: NONE

Study Groups

PK and Safety

A Single 6-hour Treatment, Pharmacokinetic and Safety Study of Natroba (spinosad) Topical Suspension 0.9% w/w in Subjects 1 Month to 3 Years 11 Months of Age with an Active Scabies Infestation.

Group Type: EXPERIMENTAL

Spinosad Topical

Intervention Type: DRUG

A topical suspension indicated for the treatment of scabies is used for this PK and Safety Study

Interventions

Spinosad Topical

A topical suspension indicated for the treatment of scabies is used for this PK and Safety Study

Intervention Type: DRUG

Other Intervention Names

Natroba; benzyl alcohol

Eligibility Criteria

Inclusion Criteria

1. Male or female, ages 1 month to 3 years and 11 months.

2. Must have active scabies infestation confirmed by clinical signs and symptoms (evidence of burrows or presence of scabies inflammatory/non-inflammatory lesions and pruritus) as well as by burrow ink test (BIT) to demonstrate the presence of burrowing mites.

3. Generally, in good health based on medical history and clinical assessments.

4. Normal-appearing skin in non-infested areas.

5. No history of chronic or recurrent dermatologic disease.

6. Willingness to comply with the study procedures including blood collections and application of study treatment in-clinic.

Exclusion Criteria

1. Presence of crusted scabies (Norwegian scabies).

2. Allergies or intolerance to ingredients in the Investigational Product.

3. Known renal or hepatic impairment.

4. Treatment with scabicide within the prior 2 weeks.

5. Immunodeficiency (including HIV infection) as reported in Medical History.

6. Signs or symptoms of systemic infection.

7. Administration of systemic therapy for infectious disease within the prior 2 weeks.

8. Receipt of any investigational product within the prior 4 weeks.

9. Medications used for itching or other indication that contain benzyl alcohol or other alcohols within the past 7 days.

10. Over-the-counter cortisone products within the past 7 days.

11. Oral prescription medications and/or antibiotics within the past 7 days.

12. Any other conditions that, at the investigator's discretion, may interfere with the study conduct, or which might confound the interpretation of the study results, or which may put the subject at undue risk.

• Minimum Eligible Age: 1 Month
• Maximum Eligible Age: 4 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Concentrics Research

OTHER

Sponsor Role: collaborator

Iqvia Pty Ltd

INDUSTRY

Sponsor Role: collaborator

Medpace, Inc.

INDUSTRY

Sponsor Role: collaborator

Inotiv Laboratories

UNKNOWN

Sponsor Role: collaborator

BioAgilytix

UNKNOWN

Sponsor Role: collaborator

Cipher Pharmaceuticals Inc.

INDUSTRY

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Sharda Angl

Role: STUDY_DIRECTOR

Cipher Pharmaceuticals Inc.

Julie Aker, MT(ASCP)

Role: STUDY_CHAIR

Concentrics Research

William Miller, MD

Role: PRINCIPAL_INVESTIGATOR

Concentrics Research

Locations

L&C Professional Medical Research Institute

Miami, Florida, United States

Site Status: RECRUITING

Velocity Clinical Research

Lafayette, Louisiana, United States

Site Status: RECRUITING

Elixir Research Group

Houston, Texas, United States

Site Status: RECRUITING

Countries

United States

Central Contacts

Sharda Angl

Role: CONTACT

sangl@cipherpharma.com

905-602-5840 ext. 267

Nina Garrett

Role: CONTACT

nina.garrett@concentricsresearch.com

800-800-5525

Facility Contacts

Maylen Perez

Role: primary

mperez@pmedresearch.com

305-269-1616

Liagnys Garcia

Role: backup

lgarciarn@pmedresearch.com

305-269-1616

Mary Long

Role: primary

mlong@velocityclinical.com

337-451-0663

DeAnna Seamester

Role: backup

dseamester@velocityclinical.com

337-451-0663

Favor Emesiani

Role: primary

f.emesiani@elixirrg.com

832-310-4750

Anita Ehidiamen

Role: backup

a.jumai@elixirrg.com

832-310-4750

Other Identifiers

SPN-110-21

Identifier Type: -

Identifier Source: org_study_id