Evaluation of EB01 Cream for the Treatment of Chronic Allergic Contact Dermatitis

Completed · Phase 2 · Has a placebo group

Conditions studied: Allergic Contact Dermatitis

In brief

The purpose of this study is to evaluate the safety and efficacy of EB01 Cream (0.2%, 1.0%, 2.0%) applied twice per day (BID) for the treatment of moderate to severe chronic allergic contact dermatitis (ACD). The purpose of the open label extension is to assess the long-term safety, tolerability, and efficacy of EB01 2.0% cream in subjects with moderate to severe chronic allergic contact dermatitis.

Key facts

Study ID

NCT03680131

Run by

Edesa Biotech Inc.

People needed

211

Starts

2019-10-15

Expected to finish

2023-01-17

Last updated by the study team

2024-11-14

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: accepted.

You may qualify if…

• All subjects:
• Men and women ≥ 18 years old, inclusive, at the time of consent.
• For women of childbearing potential involved in any sexual intercourse that could lead to pregnancy: the subject must agree to use an effective contraceptive method from at least 4 weeks before Day 1 until at least 4 weeks after the last study product application. Effective contraceptive methods include hormonal contraceptives (combined oral contraceptive, patch, vaginal ring, injectable, or implant), intrauterine devices or intrauterine systems, vasectomized partner(s), tubal ligation, or a barrier method of contraception (male condom, female condom, cervical cap, diaphragm, contraceptive sponge) in conjunction with spermicide.
• Note: Subjects must have been on a stable dose of hormonal contraceptives for at least 4 weeks before Day 1.
• Note: The above list of contraceptive methods does not apply to subjects who are abstinent for at least 4 weeks before Day 1 and will continue to be abstinent from penile-vaginal intercourse throughout the study. The reliability of sexual abstinence needs to be evaluated in relation to the duration of the clinical trial and the preferred and usual lifestyle of the participant.
• Note: A woman of nonchildbearing potential is as follows:
• Woman who has had surgical sterilization (hysterectomy, bilateral oophorectomy, or bilateral salpingectomy);
• Woman who has had a cessation of menses for at least 12 months without an alternative medical cause, and a follicle-stimulating hormone (FSH) test confirming nonchildbearing potential (refer to laboratory reference ranges for confirmatory levels).
• For men involved in any sexual intercourse that could lead to pregnancy, subject must agree to use one of the effective contraceptive methods listed in Inclusion Criterion #2 from Day 1 until at least 4 weeks after the last study product application. If the female partner of a male subject use any of the hormonal contraceptive methods listed above, this contraceptive method must be used by the female partner from at least 4 weeks before Day 1 until at least 4 weeks after the last study product application.
• Female of childbearing potential has had a negative pregnancy test at screening visit.
• Subject is willing to participate and is capable of giving informed consent. Note: Consent must be obtained prior to any study-related procedures.
• Subjects must be willing to comply with all study procedures and must be available for the duration of the study.
• HV only:
• Subject is in good general health, according to the investigator's judgment based on medical history and physical examination/laboratory/ECG/vital signs assessments.
• Subjects with allergic contact dermatitis only:
• Subject has at least 3-month history of allergic contact dermatitis (information obtained from medical chart or subject's physician, or directly from the subject).
• Subject has moderate to severe chronic allergic contact dermatitis at Day 1, defined by either one of the following:
• CDSI score ≥ 7
• CDSI score of severe (3) in ≥ 2 of the 5 assessed symptoms (Fissures, Scaling, Redness, Pruritus, Dryness)
• Subject has allergic contact dermatitis covering between 0.5% to 10% of the total BSA at Day 1.
• Subject has an ISGA ≥ 3 at Day 1.
• The subject has had a positive patch test ("+", "++" or "+++" reaction) to an allergen that is suspected to be involved in the current allergic contact dermatitis in the past 5 years (obtain written documentation of patch test result if possible).
• Alternatively, the Subject agrees to undergo patch testing during the study period (patch testing needs to be completed by Day 36). Guidelines for patch test interpretation are provided in Appendix 2. The measure of the degree of the reaction will be determined on the basis of the reading 2 and 3-4 days post application.
• Subject agrees to only apply personal care products (i.e. makeup and eyeshadow) that do not contain their allergen(s) on lesions only after applying the IP.
• Subject agrees not to apply any personal care products on allergic contact dermatitis lesions prior to site visits.

You may not qualify if…

• All subjects:
• Subject is a female who is breastfeeding, pregnant, or who is planning to become pregnant during the study.
• Current or recurrent disease, other than allergic contact dermatitis (applicable to subject with allergic contact dermatitis only), that could affect the action, absorption, or disposition of the study drug, or clinical or laboratory assessments.
• Subject has a history of skin disease or presence of skin condition, other than allergic contact dermatitis (applicable to subject with allergic contact dermatitis only) that, in the opinion of the investigator, would interfere with the study assessments.
• Subject is known to have immune deficiency or is immunocompromised.
• Subject has a history of cancer or lymphoproliferative disease within 5 years prior to Day 1. Subjects with successfully treated non-metastatic cutaneous squamous cell or basal cell carcinoma and/or localized carcinoma in situ of the cervix are not to be excluded.
• Subject had a major surgery within 8 weeks prior to Day 1 or has a major surgery planned during the study.
• Subject has any clinically significant medical condition that would, in the opinion of the investigator, put the subject at undue risk or interfere with interpretation of study results.
• Subject has a known history of chronic infectious disease (e.g., hepatitis B, hepatitis C, or infection with human immunodeficiency virus).
• Subject has used systemic treatments (other than biologics) that could affect allergic contact dermatitis (applicable to subjects with allergic contact dermatitis only) or is known to cause cutaneous irritation or sensitization reactions less than 2 weeks prior to Day 1 (e.g., oral/injectable corticosteroids, retinoids, calcineurin inhibitors, methotrexate, cyclosporine, hydroxycarbamide [hydroxyurea], azathioprine) Note: Intranasal corticosteroids and inhaled corticosteroids for stable medical conditions are allowed. Eye drops containing corticosteroids are allowed.
• Use of any prescription or over-the-counter (OTC) medication that, in the opinion of the Principal Investigator, could affect (improve or worsen) the allergic contact dermatitis condition or is known to cause cutaneous irritation or sensitization reactions.
• Subject has received any marketed or investigational biological agent within 12 weeks or 5 half-lives (whichever is longer) prior to Day 1.
• Subject is currently receiving a nonbiological investigational product or device or has received one within 2 weeks prior to Day 1.
• Subject has received any UV-B phototherapy (including tanning beds) or excimer laser within 2 weeks prior to Day 1.
• Subject had excessive sun exposure, is planning a trip to a sunny climate, or has used tanning booths within 2 weeks prior to Day 1 or is not willing to minimize natural and artificial sunlight exposure during the study. Use of sunscreen products and protective apparel are recommended when exposure cannot be avoided. If sunscreen is applied to ACD lesions, it should be applied after the IP.
• Subject has a known hypersensitivity to EB01 or its excipients.
• Subject has uncontrolled diabetes.
• Subject has a known history of clinically significant drug or alcohol abuse in the last year prior to Day 1.
• HV only:
• Subject has history of recurrent chronic or presence of allergic contact dermatitis.
• Subject has used any medicated topical product on the face within 2 weeks prior to Day 1.
• Subjects with allergic contact dermatitis only:
• Subjects with active atopic dermatitis lesions overlapping with allergic contact dermatitis lesions at Day 1.
• Subject has clinically infected allergic contact dermatitis lesions (bacterial, viral, or fungal).
• Subject has allergic contact dermatitis on lips or mucous membranes only.

Where it is running

• Ark Clinical Research — Long Beach, California, United States
• Foxhall Dermatology — Washington D.C., District of Columbia, United States
• Gold Coast Dermatology — Delray Beach, Florida, United States
• Miami Dade Medical Research Institute, LLC — Miami, Florida, United States
• The Dermatology Centre of Indiana — Plainfield, Indiana, United States
• Forefront Dermatology — Louisville, Kentucky, United States
• The Dermatology Clinic — Baton Rouge, Louisiana, United States
• Oakland Hills Dermatology P.C. — Auburn Hills, Michigan, United States
• Associated Skin Care Specialists — Fridley, Minnesota, United States
• JUVA Skin & Laser Center — New York, New York, United States
• UNC Dermatology and Skin Cancer Center — Chapel Hill, North Carolina, United States
• Bexly Dermatology — Bexley, Ohio, United States
• Apex Clinical Research Center, LLC — Mayfield Heights, Ohio, United States
• West Virginia Research Institute — Morgantown, West Virginia, United States
• Lynderm Research Inc. — Markham, Ontario, Canada

Full record on ClinicalTrials.gov

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