Efficacy and Tolerability of HAT1 Compared to Calcipotriol in Patients With Mild to Moderate Chronic Plaque Psoriasis
Study Details
Study Description
Brief Summary
Psoriasis, the most prevalent autoimmune disease in the U.S., manifests with plaque type psoriasis vulgaris with lesions localized to the scalp, postauricular region, face, diaper area, elbows, and knees. Inadequately controlled disease is common and a significant cause of extensive psychological and clinical morbidity in children. In addition, the safety and tolerability issues of common treatments for psoriasis including topical corticosteroids, calcipotriol, oral cytotoxic drugs, and biologic agents are especially problematic in patients that limit their use. Identification of therapies with high efficacy and safety profiles suitable for patients with psoriasis is therefore an area of critical unmet need. Haus Bioceuticals has developed a topical treatment for psoriasis denoted HAT1 (based on ingredients that have established clinical benefit), and further have demonstrated that HAT1 is safe and profoundly effective in the treatment of psoriasis. This study is aimed to further evaluate the efficacy and safety of HAT1 compared to commonly used calcipotriol in patients with mild to moderate chronic plaque psoriasis.
| Condition or Disease | Intervention/Treatment | Phase |
|---|---|---|
|
Phase 1/Phase 2 |
Detailed Description
This study is an exploratory 10-week open-label clinical study designed to evaluate the efficacy and safety of HAT1 when compared to calcipotriol in adult patients with mild to moderate chronic plaque psoriasis. The study will include subjects with ages 18 - 65 years old inclusive. Group assignments will be balanced by disease severity, age, and body location of lesions. The study will consist of a 1 week washout period and a 12 week treatment phase. During the treatment phase, subject will be provided one of the two labeled test products HAT1 or calcipotriol to use twice daily on all lesions and non-lesional areas as instructed. No additional creams, lotions or soaps other than provided test products will be allowed throughout the duration of the study. There will also be consumption/compliance checks and dermatological evaluations at each visit.
Study Design
Arms and Interventions
| Arm | Intervention/Treatment |
|---|---|
| Experimental: HAT1 topical solution HAT1 topical solution will come in a labeled spray bottle. This topical medicated solution will be applied once in the morning and once in the evening at least 8 hours apart to all lesions. Treatment will continue daily until next visit. |
Drug: HAT1 topical solution
HAT1 topical solution will be applied twice daily. The research team will provide instructions for the correct application of the treatment. If a lesion disappears, patients will continue applying the cream twice daily to the area. No additional creams, lotions or soaps other than provided test products will be allowed throughout the duration of the study.
Other Names:
|
| Active Comparator: Calcipotriol ointment (0.005%) Calcipotriol ointment (0.005%) will come in a labeled tube. The medicated cream will be be applied once in the morning and once in the evening at least 8 hours apart to all lesions. Treatment will continue daily until next visit. |
Drug: Calcipotriol
Calcipotriol ointment (0.005%) will be applied twice daily. The research team will provide instructions for the correct application of the treatment. If a lesion disappears, patients will continue applying the cream twice daily to the area. No additional creams, lotions or soaps other than provided test products will be allowed throughout the duration of the study.
Other Names:
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Outcome Measures
Primary Outcome Measures
- Percentage of patients who achieve a Psoriasis Area and Severity Index (PASI) 75 response [[Time Frame: Baseline to week 12]]
Secondary Outcome Measures
- Percentage of patients achieving a Physicians Global Assessment (PGA) of Clear or Minimal at Week 12 [[Time Frame: Baseline to week 12]]
- Incidence of treatment emergent adverse events [[Time Frame: baseline to week 12]]
Eligibility Criteria
Criteria
Inclusion Criteria:
- Clinical diagnosis of psoriasis with a psoriasis area and severity index (PASI) score
3 and < 12
-
Treatment area amenable to topical treatment
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Attending a hospital outpatient clinic or the private practice of a dermatologist
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Males or Females between 18-65 years
Exclusion Criteria:
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Systemic treatment with immunosuppressive drugs or corticosteroids within 4 weeks prior to enrollment. (Inhaled or intranasal steroids for asthma or rhinitis may be used)
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Topical treatment with immunomodulators or corticosteroids within 4 weeks prior to enrollment.
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Phototherapy therapy within 4 weeks prior to enrollment or other topical therapy on the treatment area within 1 week prior to enrollment.
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Patients requiring any other topical or systemic medications that could affect the course of psoriasis during the study period.
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Clinical infection on the treatment area or patients with history of cancer including skin cancer, history of an immunocompromised disease.
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Current participation in any other interventional clinical trial
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History of allergy of any components in HAT1 or previously treated with HAT1
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Subjects with intense sun exposure during the study
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Patients known or suspected of not being able to comply with a trial protocol (e.g. alcoholism, drug dependency, or psychotic state)
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Patients that are currently pregnant or lactating or planning to become pregnant in the next 6 months
Contacts and Locations
Locations
No locations specified.Sponsors and Collaborators
- Haus Bioceuticals
Investigators
None specified.Study Documents (Full-Text)
None provided.More Information
Publications
None provided.- HCTP2211A