A Trial of a Botanical Drug Containing East Indian Sandalwood Oil (EISO) For Treatment of Atopic Dermatitis

Completed · Phase 2 · Has a placebo group

Conditions studied: Atopic Dermatitis, Eczema

In brief

This trial will be a double-blind, randomized, placebo-controlled, safety, tolerability and efficacy trial of SAN007 (5% East Indian sandalwood oil in a cream formulation) treatment regimen when administered daily for up to 28 days to patients at least 18 years of age, with atopic dermatitis.

Key facts

Study ID: NCT02871479
Run by: Santalis Pharmaceuticals, Inc.
People needed: 71
Starts: 2017-04-21
Expected to finish: 2018-08-31
Last updated by the study team: 2019-05-29

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

Subjects will be included in the trial if they meet all of the following criteria:
Are at least 18 years of age
Have atopic dermatitis, as determined by an EASI score of ≥5 and ≤50 (Hanifin, 2001)
Total treatment area(s) of atopic dermatitis involvement ≥2% and ≤15% today surface area (BSA).
Have atopic dermatitis that has been clinically stable for ≥ 30-days prior to the Screening Visit.
Are able to obtain written informed consent/ascent in a manner approved by the Institutional Review Board and comply with the requirements of the study.
Are willing to refrain from using any lotions, moisturizer, cleansers, cosmetics or creams, other than those issued as part of the study, on the target treatment areas during the treatment period.
Are free of any systemic or dermatologic disorder, which, in the opinion of the investigator, will interfere with the study results or increase the risk of adverse events.
Are willing to refrain from exposure to artificial ultraviolet radiation for the duration of the study.
Are willing to cover target treatment areas to avoid exposure to natural ultraviolet radiation for the duration of the study.
If female of childbearing potential, must be willing to practice an acceptable form of birth control for the duration of the study. i.e. barrier method, hormone or intrauterine device.
Are willing to avoid participation in any other interventional clinical trial for the duration of this study.
Are willing to refrain from treating areas that are not in the defined treatment area(s), which will be excluded from the IGA assessments and BSA calculation. These areas are as follows: head, neck, soles of feet, palms of hands, axillae, or intertriginous areas.

You may not qualify if…

Subjects will be excluded from the trial if they meet any of the following criteria:
Have a sibling or immediate family member already participating in this trial.
Currently requires and/or, in the 30 days prior to Screening, has required topical use of a medium or high potency steroid (i.e. >1%)
Atopic dermatitis that, in the opinion of the investigator, is likely to stem from an allergic reaction. (i.e. contact dermatitis)
Have <2% or >15% total BSA of atopic dermatitis involvement in the target treatment area(s).
Have participated in any interventional clinical trial in the previous 30 days to the screening visit.
Have a known sensitivity to any of the constituents of the test product including sensitivities to sandalwood oil, fragrances or any member of the Compositae family of vascular plants (e.g., sunflowers, daisies, dahlias, etc.).
Have received phototherapy within the 60 days prior to Screening.
Have received any systemic medication for atopic dermatitis in the past 2 months that would interfere with the evaluation of atopic dermatitis (excluding antihistamines or leukotriene inhibitors).
Have a present condition or abnormality that in the opinion of the Investigator would compromise the safety of the patient or the quality of the data.
Are pregnant, breast-feeding or plan to become pregnant at any point for the duration of the trial.
Are not willing to practice an approved form of birth control while on the study drug for the duration of the trial. i.e. barrier method, hormone or intrauterine device.
Have been treated, with prescription medication for atopic dermatitis, within 60 days prior to the Baseline visit.
Have any evidence of systemic cancer, squamous cell carcinoma, basal cell carcinoma, in the last 5 years,or any other confounding skin condition.
Have undergone treatments with topical atopic dermatitis drug products, other than retinoids or corticosteroids, within 14 days prior to the Baseline Visit, and for therapy containing corticosteroids or retinoids within 28 days prior to Baseline Visit.
Have open sores or open lesions in the treatment area(s).
Have a history of alcohol or illegal drug/substance abuse, or suspected alcohol or illegal drug/substance abuse in the past 2 years.
Require greater than 2.0 mg/day inhaled or intranasal corticosteroids.
Have an active infection of any kind at Visit 1 (Baseline)
Have an occupation that requires ≥50% of time be spent outdoors, where prolonged exposure to ultraviolet radiation is unavoidable.

Where it is running

DermResearch — Austin, Texas, United States
J&S Sudies Pharmaceutical — Bryan, Texas, United States
Progressive Clinical Research — San Antonio, Texas, United States
Texas Dermatology and Laser Specialists — San Antonio, Texas, United States
Clinical Trials of Texas — San Antonio, Texas, United States

Full record on ClinicalTrials.gov

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