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Phase 4 N=20 Randomized Triple-blind Treatment

A Study for a Topical Medication Versus Placebo in Patients With Hand Dermatitis

Hand Dermatitis

Enrolled (actual)
20
Serious AEs
0.0%
Results posted
Nov 2022
Primary outcome: Primary: Primary Outcome Measure for Efficacy (IGA) — 2.33; 2.20; 2.43; 2 score on a scale

Study Design & Population

Study type
Interventional
Phase
Phase 4
Interventions
Topical AFX5931 (Drug); Topical Placebo (Drug)
Age
Pediatric, Adult, Older Adult · 12+ yrs
Sex
All
Sponsor
The Center for Clinical and Cosmetic Research
Primary completion
Apr 2019

Outcome Measures

OutcomeResultp-value
PRIMARY
Primary Outcome Measure for Efficacy (IGA)
2.33; 2.20; 2.43; 2; 2.20; 2.25
PRIMARY
Primary Outcome Measure for Efficacy (HECSI)
22.67; 25.6; 20.8; 20; 20.6; 21
SECONDARY
Secondary Outcome Measures for Tolerability and Safety (Tolerability Assessment - Pruritus Score)
1.53; 1.8; 1.29; 1; 0.93; 1
SECONDARY
Secondary Outcome Measures for Tolerability and Safety (LSR)
1.33; 1.4; 1.36; 1; 1.27; 1.25
SECONDARY
Measures for Safety (Adverse Events/Concomitant Medications)
0; 0; 0; 0; 0; 0

Summary

This is a double-blind, pilot study with 20 subjects to determine the tolerability and efficacy of topical AFX 5931 in the treatment of mild to moderate hand dermatitis. Subjects are screened up to 30 days before the baseline visit. Subjects who meet the eligibility criteria may qualify for the study. Subjects will be randomized in a 3:1 ratio to receive either the active or vehicle medication. 15 subjects will receive the active, therapeutic product and 5 subjects will receive the inactive, vehicle product.

Eligibility Criteria

Inclusion Criteria

  • Subject is a male or non-pregnant female, 12 years of age and older.
  • Subject is willing and able to provide written informed consent for the study.
  • Subject is willing and able to apply the investigational product as directed, comply with study instructions and commit to all follow-up visits for the duration of the study.
  • Subject has clinical diagnosis of mild to moderate hand dermatitis for at least 3 months.
  • Subject has a baseline Investigator's Global Assessment (IGA) score of 2 or 3 (disease severity of mild or moderate).
  • Subject is in good general health and free of any disease state or physical condition that might impair evaluation of hand dermatitis or which, in the investigator's opinion, exposes the subject to an unacceptable risk by study participation.
  • Women of childbearing potential (WOCBP) must use an effective method of birth control or must be post-menopausal or surgically sterile. Women of childbearing potential (WOCBP) must have a negative urine pregnancy test (UPT) at Baseline.

Exclusion Criteria

  • Subject is pregnant, lactating, or is planning to become pregnant during the study.
  • Subject is currently enrolled in an investigational drug or device study.
  • Subject has used an investigational drug or investigational device treatment within 30 days prior to Visit 2/Baseline.
  • Subject has active cutaneous bacterial or viral infection in any treatment area (clinically infected hand dermatitis) at Visit 2/Baseline.
  • Subject has used any of the following therapies within 30 days prior to Visit 2/Baseline:
  • Systemic corticosteroids (oral and injectable [intravenous and intramuscular]) (Intranasal and Inhalational steroids are allowed if use is kept constant during the study)
  • UVA/UVB therapy
  • PUVA (psoralen plus ultraviolet A) therapy
  • Immunomodulators or immunosuppressive therapies
  • Interferon
  • Cytotoxic drugs (e.g., methotrexate, cyclophosphamide, azathioprine)
  • Oral retinoids
  • Subject has used any of the following therapies within 14 days prior to Visit 2/Baseline:
  • Systemic antibiotics
  • Topical calcipotriene or other topical vitamin D preparations
  • Subject has used any of the following therapies within 7 days prior to Visit 2/Baseline: • Topical and oral antihistamines
  • Topical antibiotics
  • Topical corticosteroids
  • Topical antifungals
  • Subject has a history of sensitivity to any of the ingredients in the investigational product
  • Subject is known to be noncompliant or is unlikely to comply with the requirements of the study protocol (e.g., due to alcoholism, drug dependency, mental incapacity) in the opinion of the investigator.
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT03703895). 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.

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