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A Phase 2, Randomized, Double-Blind, Placebo-Controlled Study to Investigate the Efficacy and Safety of LY3972406 in Adults With Moderate-to-Severe Plaque Psoriasis
The main purpose of this study is to determine the efficacy and safety of LY3972406 in adult participants with moderate-to-severe plaque psoriasis.
Age
18 - 75 years
Sex
ALL
Healthy Volunteers
No
Dermatology Research Associates
Los Angeles, California, United States
Clinical Science Institute
Santa Monica, California, United States
Driven Research
Coral Gables, Florida, United States
Conquest Research
Winter Park, Florida, United States
Psoriasis Treatment Center of Central New Jersey
East Windsor, New Jersey, United States
Schweiger Dermatology Group
Hackensack, New Jersey, United States
Metropolitan Dermatology - Clark
Kenilworth, New Jersey, United States
Accellacare - Winston-Salem
Winston-Salem, North Carolina, United States
Remington-Davis, Inc
Columbus, Ohio, United States
DermDox Centers for Dermatology
Camp Hill, Pennsylvania, United States
Start Date
December 6, 2023
Primary Completion Date
April 1, 2025
Completion Date
May 6, 2025
Last Updated
October 15, 2025
33
ACTUAL participants
LY3972406
DRUG
Placebo
DRUG
Lead Sponsor
Eli Lilly and Company
NCT07116967
NCT07250802
NCT07449702
Data Source & Attribution
This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.
Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.
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