A Study to Determine the Safety & Efficacy of ZPL-5212372 in Healthy Subjects and in Subjects With Atopic Dermatitis

Ziarco Pharma

Status and phase: Completed; Phase 2; Phase 1

Conditions: Atopic Dermatitis

Treatments: Drug: ZPL-5212372 1% w/w Ointment BID; Drug: Placebo Ointment BID

Study type: Interventional

Funder types: Industry

Identifiers

NCT02795832

Ziarcopharma

Details and patient eligibility

About

A Randomised, Adaptive Design, Double-Blind (3rd Party Open), Placebo Controlled, Sequential Group Study to Determine the Safety,Tolerability, Pharmacokinetics and Efficacy of Twice Daily Application of a Topical ZPL-5212372 (1.0% w/w) Ointment Administered for up to 2 Weeks in Adult Healthy Volunteers and Patients with Moderate to Severe Atopic Dermatitis

Full description

This study was a randomised, adaptive design, double blind (3rd party open), placebo controlled, sequential group study in both healthy volunteers and patients with moderate to severe AD. This study was divided into 3 separate, sequential cohorts:

• Cohort 1 were to assess safety, toleration and pharmacokinetics (PK) with intensive monitoring as in-patients over 7 days of dosing in healthy volunteers.
• Cohort 2 were to assess safety, toleration and PK with intensive monitoring as in-patients over 7 days of dosing in moderate to severe AD patients.
• Cohort 3 were to assess efficacy, safety, toleration and PK as out-patients over 14 days of dosing in moderate to severe AD patients.

Subjects received 1.0% (w/w) ZPL-5212372 or matched placebo ointment topically, twice daily.

Enrollment: 53 patients

Sex: All

Ages: 18 to 65 years old

Volunteers: Accepts Healthy Volunteers

Inclusion criteria

• Healthy males or females, aged between 18 and 55 years, inclusive (healthy is defined as no clinically relevant abnormalities identified by a detailed medical history, full physical examination, including blood pressure and pulse rate measurement, 12-lead ECG and clinical laboratory tests).

or

Males and females aged 18-65 years inclusive with physician documented history or diagnosis of atopic dermatitis for at least 6 months prior to screening. AD should be diagnosed by the Eichenfield revised criteria of Hanifin and Rajka.

For Atopic Dermatitis Patients:

Eczema Area and Severity Index (EASI) of ≥9 and <48 at Screening and an EASI of ≥12 and <48 at Day 1.

An Investigator's Global Assessment (IGA) score ≥ 3 at both Screening and Day 1.

Atopic dermatitis affecting between ≥10 to <40% BSA at Screening and ≥10% to <50% BSA on Day 1.

All Subjects:

Evidence of a personally signed and dated informed consent form, indicating that the subject has been informed of all pertinent aspects of the study.

Exclusion criteria

For Healthy Subjects

• Evidence or history of clinically significant haematological, renal, endocrine, pulmonary, gastrointestinal, cardiovascular, hepatic, psychiatric, neurologic, or allergic disease (including drug allergies, but excluding untreated, asymptomatic, seasonal allergies at time of dosing).
• Have tattoos covering areas of skin to be dosed with study ointment.
• Subjects who are hirsute in areas of skin to be dosed with study ointment.
• Subjects who have received treatment with an investigational drug within 3 months prior to screening.

For Atopic Dermatitis Patients:

• AD of such severity (EASI >48) that the subject could not comply with the demands of the study and/or the subject is not a suitable candidate for a placebo-controlled study.
• Have concomitant skin disease or infection (e.g. acne, impetigo) or presence of skin comorbidities in the study area to be dosed that may interfere with study assessments.
• Have received phototherapy (e.g. UVA, UVB or PUVA therapy), or systemic therapy (e.g. immunosuppressants [such as cyclosporine, azathioprine, methotrexate], cytostatics) known or suspected to have an effect on AD, within 4 weeks of the start of the study. All other biologics should not have been used within 3 months of the start of study.
• Have received systemic corticosteroids (e.g. oral, intravenous, intraarticular, rectal) within 4 weeks of the start of the study. Subjects on a stable maintenance dose (over the preceding 3 months) of inhaled or intranasal CS may participate.
• Patients treated with oral antihistamines or topical calcineurin inhibitors or topical steroids within 7 days of starting study; intranasal antihistamines for the treatment of allergic rhinitis are acceptable.

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: Quadruple Blind

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53 participants in 6 patient groups, including a placebo group

Cohort 1a

Experimental group

Description:

ZPL-5212372 1% w/w Ointment BID

Treatment:

Drug: ZPL-5212372 1% w/w Ointment BID

Cohort 1b

Placebo Comparator group

Description:

Placebo Ointment BID

Treatment:

Drug: Placebo Ointment BID

Cohort 2a

Experimental group

Description:

ZPL-5212372 1% w/w Ointment BID

Treatment:

Drug: ZPL-5212372 1% w/w Ointment BID

Cohort 2b

Placebo Comparator group

Description:

Placebo Ointment BID

Treatment:

Drug: Placebo Ointment BID

Cohort 3a

Experimental group

Description:

ZPL-5212372 1% w/w OIntment BID

Treatment:

Drug: ZPL-5212372 1% w/w Ointment BID

Cohort 3b

Placebo Comparator group

Description:

Placebo Ointment BID

Treatment:

Drug: Placebo Ointment BID