A Study of LY4100511 (DC-853) in Adult Participants With Moderate-to-Severe Plaque Psoriasis
Plaque PsoriasisThe main purpose of this study is to assess the safety and efficacy of LY4100511 in adult participants with moderate-to-severe plaque psoriasis.
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Participation Requirements
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Sex:
ALL -
Eligible Ages:
18 to 70
Participation Criteria
Inclusion Criteria:
* Clinical diagnosis of plaque psoriasis for 6 months before the baseline day 1 randomization
* Must have a body mass index (BMI) of 18 to 40 kilogram/square meter (kg/m2) (inclusive).
* Must be willing to discontinue topical and/or systemic therapies for psoriasis before the first dose of study intervention.
* Must agree to avoid prolonged exposure to the sun and to refrain from the use of tanning booths, sun lamps, and other sources of ultraviolet light during the study
Exclusion Criteria:
* Have had a clinically significant flare of psoriasis during the 12 weeks before the baseline, as assessed by the investigator.
* Have a history of erythrodermic psoriasis, generalized or localized pustular psoriasis, predominantly guttate psoriasis, or medication-induced or medication-exacerbated psoriasis.
* Have any known or suspected diagnosis of inflammatory conditions other than psoriasis and psoriatic arthritis, including but not limited to rheumatoid arthritis, sarcoidosis, IBD (Crohn's disease or ulcerative colitis), or systemic lupus erythematosus.
* Have a diagnosis of psoriatic arthritis requiring, or are currently receiving, systemic immunosuppressant medical treatment (including corticosteroids, immunosuppressants, and biologics).
* Have a current or recent acute, active infection. Participant must have no symptoms or signs of confirmed or suspected infection and must have completed any appropriate anti-infective treatment for at least 30 days before screening and up to randomization/baseline.
Study Location
Skin Care West
Skin Care WestNanaimo, British Columbia
Canada
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Lovegrove Dermatology - Probity - PPDS
Lovegrove Dermatology - Probity - PPDSLondon, Ontario
Canada
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Interior Dermatology Centre - Probity - PPDS
Interior Dermatology Centre - Probity - PPDSKelowna, British Columbia
Canada
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Dermatrials Research Inc.
Dermatrials Research Inc.Hamilton, Ontario
Canada
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DermEdge Research
DermEdge ResearchMississauga, Ontario
Canada
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Toronto Research Centre Inc
Toronto Research Centre IncToronto, CA
Canada
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DermEffects - Probity - PPDS
DermEffects - Probity - PPDSLondon, Ontario
Canada
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Simcoderm Medical & Surgical Dermatology Centre
Simcoderm Medical & Surgical Dermatology CentreBarrie, Ontario
Canada
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Lynderm Research Inc.
Lynderm Research Inc.Markham, Ontario
Canada
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SimcoDerm Medical and Surgical Dermatology Centre
SimcoDerm Medical and Surgical Dermatology CentreBarrie, Ontario
Canada
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- Study Sponsored By
- Eli Lilly and Company
- Participants Required
- More Information
- Study ID:
NCT06602219