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A Bioequivalence Study With Clinical Endpoints to Evaluate the Safety and Therapeutic Equivalence of Permethrin Cream 5% & Elimite™ in Subjects With Scabies

Phase 3
Completed
Conditions
Scabies
Interventions
Registration Number
NCT03973775
Lead Sponsor
Saptalis Pharmaceuticals LLC
Brief Summary

This phase III study was conducted to establish the clinical bioequivalence of Permethrin Cream 5% and Elimite™ in the treatment of scabies following a single application.

Detailed Description

A Double Blind, Two Arm, Multicenter, Randomized, Parallel Group Bioequivalence Study with Clinical Endpoints to Evaluate the Safety and Therapeutic Equivalence of, Permethrin Cream 5% (Manufactured by Saptalis Pharmaceuticals, LLC) \& Elimite™ (Permethrin Cream 5%, manufactured for Prestium Pharma, Inc.) in Subjects with Scabies.

The objectives of this study are:

Primary Objective: To establish the clinical bioequivalence of Permethrin Cream 5% (manufactured by Saptalis Pharmaceuticals, LLC) and Elimite™ (Permethrin Cream 5%, manufactured for Prestium Pharma, Inc.) in the treatment of scabies (Sarcoptes scabiei) following a single application.

Secondary Objective: To compare the safety and tolerability between the study drugs.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
126
Inclusion Criteria
  • Subjects and/or parent/guardian must have understood and signed appropriately administered informed consent/assent in their own language
  • Healthy male and non-pregnant/non-lactating female subjects aged 2 months to 65 years diagnosed with scabies
  • Must have dermatological evidence of active scabies (burrows, erythematous papules, etc.) confirmed by recovery of live Sarcoptes scabiei (the Principal investigator or trained and experienced Study Team examines the specimen(s) under magnification to verify the identity and viability of the scabies mite, ova, or mite feces at the site)
  • The youngest subject (with scabies infestation as defined above) from each household is considered the index or primary subject of the household for evaluation of the primary endpoint. Other members of the household and close contacts are enrolled in the study as Secondary subjects and evaluated for all safety parameters (not included in primary endpoint analysis). Secondary subjects that are confirmed to have dermatological evidence of scabies should receive the same study treatment as the Index subject
  • Must be available and willing to report for follow up visits
  • Is otherwise healthy, well-nourished, non-febrile and not suffering from an infection likely to require systemic antibiotic or topical therapy. These criteria will be ascertained during screening by the Principal investigator
  • Must agree not to use other scabicides or other medications likely to affect the evaluation of their response to scabies treatment
  • If female of childbearing potential, willing to use an acceptable method of birth control, should be stable for 3 months prior to screening and throughout the study
  • Must be willing to follow the procedures to decrease infestation: Clothes and bed linens that were in contact with the subjects, their household members and close contacts during the previous 48 to 72 hours will be machine washed at 60°C and machine dried the day after the first treatment. For materials that cannot be laundered, insecticide powder or aerosolized insecticide may be used, or the items may be kept in a sealed bag for at least 48 to 72 hours.
Exclusion Criteria
  • Subject or parent/guardian has not signed informed consent/assent
  • Pregnant females, lactating females or females planning for a pregnancy
  • Females of childbearing potential who do not agree to utilize an adequate method of contraception
  • Known history of irritation or sensitivity to parasiticides
  • Skin conditions that could make it difficult to evaluate the extent of an infestation or would present a problem in the evaluation of response to therapy (e.g. atopic dermatitis, eczema, contact dermatitis, lichen planus, papular urticaria, seborrheic dermatitis).
  • Use within 4 weeks of baseline visit (1) immunomodulators (2) systemic medications that suppress the immune system (3) topical or oral parasiticides.
  • Use within 2 weeks of baseline visit (1) topical steroids (2) topical or systemic antibiotics
  • Has crusted scabies • Known allergy or hypersensitivity to permethrin, any synthetic pyrethroid or pyrethrin, plants in the Asteraceae/Compositae family (e.g. chrysanthemums, ragweed, marigolds, and daisies)
  • Subjects whose household members and close contacts refuse treatment.
  • Subjects with greater than 5 infested household members and close contacts
  • Subjects whose sexual contacts do not agree to restrict prolonged skin to skin contact with non-household members during the study period
  • Subjects with a household member less than 2 months of age
  • Suffers from a renal or hepatic impairment
  • Has been treated for scabies by any form of scabies treatment whether prescription, over-the-counter or a home remedy within a month prior to their screening visit
  • Had received or used an investigational new drug within the month immediately preceding the screening
  • Is receiving any medication likely to mask or modify scabies
  • Will not be available for follow up visits
  • Has other cutaneous conditions which might be confused with scabies
  • Seriously immune suppressed subjects
  • Has been previously empaneled in this study

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Test Drug Treatment ArmPermethrin Cream 5%Permethrin Cream 5%, Saptalis Pharmaceuticals, LLC
Reference Drug Treatment ArmPermethrin Cream 5%Elimite™ (Permethrin Cream 5%), Prestium Pharma, Inc.
Primary Outcome Measures
NameTimeMethod
The primary endpoint is the proportion of index subjects in the Per Protocol (PP) population in each treatment group with treatment cure when examined at Visit 4 (Day 28 ± 2 Days).Day 28 ± 2 Days

Cure is defined as demonstration of clinical cure (all clinical findings have completely resolved, including inflammatory/non-inflammatory lesions) and microscopic cure (demonstration of the absence of mites, ova, and/or mite feces) on Day 28. Negative microscopy can be declared if no mites, ova, or mite feces is found from a minimum of 3 skin scrapings from previously affected sites.

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (5)

Havana Research Institute

🇺🇸

Pasadena, California, United States

Universal Biopharma Research Institute Inc.

🇺🇸

Dinuba, California, United States

SouthCoast Research Center, Inc (Clinical Site & Drug Shipment Facility)

🇺🇸

Miami, Florida, United States

Long Beach Clinical Trials Services, Inc.

🇺🇸

Long Beach, California, United States

West Houston Clinical Research Service

🇺🇸

Houston, Texas, United States

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