Phase
Condition
Hives (Urticaria)
Skin Infections/disorders
Eczema (Atopic Dermatitis)
Treatment
Placebo
Prednisone
LY3872386
Clinical Study ID
Ages 18-65 All Genders Accepts Healthy Volunteers
Study Summary
Eligibility Criteria
Inclusion
Inclusion Criteria:
Part A and C:
- Overtly healthy as determined by medical evaluation
To qualify as Japanese for the purpose of this study, the participant must befirst generation Japanese, defined as the participant's biological parents andall of the participant's biological grandparents must be of exclusive Japanesedescent, and must have been born in Japan
To qualify as Chinese for the purpose of this study, the participant must be,at a minimum, third-generation Chinese, defined as all 4 of the participant'sbiological grandparents must be of exclusive Chinese descent and born in China
Have a body mass index of 18.0 to 32.0 kilograms per square meter (kg/m²), inclusive
Male participants who agree to use highly effective or effective methods ofcontraception and women not of childbearing potential may participate in part A andC
Part B:
Participants who have a diagnosis of atopic dermatitis at least 12 months prior toscreening as defined by the American Academy of Dermatology
Have a history, documented by a physician and/or investigator, of inadequateresponse to existing topical medications within 6 months preceding screening, orparticipants who failed systemic therapies intended to treat atopic dermatitis or ahistory of intolerance to topical therapy
Have a body mass index of 18.0 to 38.0 kilograms per square meter (kg/m²), inclusive
Male participants who agree to use highly effective or effective methods ofcontraception, women not of childbearing potential and women of childbearingpotential may participate in part B
Exclusion
Exclusion Criteria:
Women who are pregnant and/or lactating
Participants who have received live vaccine(s) (including attenuated live vaccines)or Bacillus Calmette- Guérin within 35 days of screening
Have a history or presence of multiple or severe allergies or an anaphylacticreaction to prescription or nonprescription drugs
Have a known history of diabetes
Have fasting glucose level of ≥126 milligrams per deciliter (mg/dL) and glycatedhemoglobin ≥6.5 percent (%) and/or taking anti-diabetes medications at screening
Have known history of osteoporosis
Study Design
Connect with a study center
Anima Research Center
Alken, Hesbaye 3570
BelgiumSite Not Available
CRU Hungary Ltd. - Early Phase Unit
Kistarcsa, Pest H-2143
HungarySite Not Available
Budai Irgalmasrendi Korhaz
Budapest, H-1027
HungarySite Not Available
Medical Corporation Heishinkai OPHAC Hospital
Osaka-shi, Osaka 532-0003
JapanSite Not Available
P-one Clinic
Hachioji, Tokyo 192-0071
JapanSite Not Available
Medicines Evaluation Unit Ltd.
Manchester, England M23 9QZ
United KingdomSite Not Available
Wythenshawe Hospital
Manchester, England M23 9QZ
United KingdomSite Not Available
Liverpool University Hospital Foundation Trust, Clinical Research Facility
Liverpool, Merseyside L7 8XP
United KingdomSite Not Available
BDD Pharma Ltd
Glasgow, Scotland G4 0SF
United KingdomSite Not Available
Glasgow Royal Infirmary
Glasgow, Scotland G4 0SF
United KingdomSite Not Available
CenExel ACT
Anaheim, California 92801
United StatesSite Not Available
Fortrea Clinical Research Unit
Daytona Beach, Florida 32117
United StatesSite Not Available
Miami Clinical Reserach
Miami, Florida 33155
United StatesSite Not Available
Skin Sciences, PLLC
Louisville, Kentucky 40217
United StatesSite Not Available
Paddington Testing Co, Inc
Philadelphia, Pennsylvania 19103
United StatesSite Not Available
Progressive Clinical Research
San Antonio, Texas 78213
United StatesSite Not Available
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