A Study of B244 Delivered as a Topical Spray to Assess Safety in Pediatric Subjects With Atopic Dermatitis

Inclusion Criteria

• Subjects are eligible to be included in the study only if all of the following criteria apply:
• Male and female subjects 2 to 17 years of age, inclusive.
• Confirmed diagnosis of atopic dermatitis according to the Hanifin and Rajka criteria.
• A minimum of 10% but no more than 60% of the subjects' body surface area (see Appendix 6 for guidance) is affected by atopic dermatitis (affected is defined by physical examination findings: erythema, edema, scaling, lichenification, and excoriation; with the excoriation serving as the physical examination correlate of pruritus).
• A vIGA-AD scale of 2 or 3 at Screening and Baseline.
• Subject, or the parent or guardian, to provide written informed consent and authorization for protected health information disclosure.
• Subjects must be generally in good health based on Investigator's assessment (other than atopic dermatitis).
• Normal vital signs, or with no clinically significant vital signs that in the opinion of the Investigator, would place the subject at increased risk or would confound the objectives of the study.
• Females must not be pregnant, as confirmed by negative urine pregnancy testing. Female subjects aged ≥11 years old, or female patients
• Clinically significant physical or mental disorder which, in the opinion of the Investigator, would place the subject at increased risk or would confound the objectives of the study.
• Subjects with atopic dermatitis on the face only.
• Active cutaneous bacterial, viral or fungal infection in any treatment area at Baseline (eg, clinically infected atopic dermatitis).
• History or presence of immunological deficiencies or diseases, organ transplant, human immunodeficiency virus (HIV), diabetes, malignancy, malignant or pre-malignant skin conditions, serious active or recurrent infection, systemic immunosuppressive regimens, clinically significant renal disease severe hepatic disorders, or other severe uncontrolled conditions (eg, drug or alcohol abuse), that are significant and/or that may pose a health risk to the subject in the study or may have an impact on the study assessments.
• Unstable atopic dermatitis or a consistent requirement for high-potency corticosteroids (class I-III steroids).
• Active systemic or localized infection (including infected AD).
• Subjects unable to comply with the excluded medication/therapy restriction
• Known hypersensitivity to the study treatment.
• Known to have hepatitis B, hepatitis C or HIV I or II tests. Details will be recorded in medical history, a blood sample will not be collected for confirmation.
• Female subject who is pregnant, breastfeeding, or considering pregnancy during the study.
• Any skin condition which in the Investigator's opinion may interfere with the evaluation of atopic dermatitis.
• Use of any investigational drugs within the previous 30 days prior to dosing or within a period of less than 5 times the drug's half-life, whichever is longer.
• Use of any biologic within a period of 5 times its half-life.
• Children or relatives of the Sponsor, clinical research organization, or the Study Site personnel are excluded from participating in the study.