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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT06176768
Other study ID # 18692
Secondary ID J4H-MC-FVAA2023-
Status Recruiting
Phase Phase 2
First received
Last updated
Start date December 6, 2023
Est. completion date July 31, 2025

Study information

Verified date February 2024
Source Eli Lilly and Company
Contact There may be multiple sites in this clinical trial. 1-877-CTLILL
Phone 1-317-615-4559
Email ClinicalTrials.gov@lilly.com
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The main purpose of this study is to determine the efficacy and safety of LY3972406 in adult participants with moderate-to-severe plaque psoriasis.


Recruitment information / eligibility

Status Recruiting
Enrollment 75
Est. completion date July 31, 2025
Est. primary completion date April 30, 2025
Accepts healthy volunteers No
Gender All
Age group 18 Years to 75 Years
Eligibility Inclusion Criteria: - Have moderate-to-severe chronic plaque psoriasis for at least 6 months prior to baseline - Have venous access sufficient to allow for blood sampling - Are able to swallow oral medication - Agree to skin biopsies Exclusion Criteria: - Have any other skin conditions, excluding plaque psoriasis - Have a current or recent acute, active infection - Have manifestations of other autoimmune diseases, such as systemic lupus erythematosus. - Are lactating or breastfeeding women

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
LY3972406
Administered orally
Placebo
Administered orally

Locations

Country Name City State
United States DermDox Centers for Dermatology Camp Hill Pennsylvania
United States Driven Research Coral Gables Florida
United States Psoriasis Treatment Center of Central New Jersey East Windsor New Jersey
United States Austin Institute for Clinical Research Houston Texas
United States Center for Clinical Studies Houston Texas
United States Metropolitan Dermatology - Clark Kenilworth New Jersey
United States Dermatology Research Associates Los Angeles California
United States Clinical Science Institute Santa Monica California
United States Accellacare - Winston-Salem Winston-Salem North Carolina
United States Conquest Research Winter Park Florida

Sponsors (1)

Lead Sponsor Collaborator
Eli Lilly and Company

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Percentage of Participants Achieving Psoriasis Area and Severity Index (PASI 75) Week 12
Secondary Mean Change from Baseline in Body Surface Area (BSA) Baseline, Week 12
Secondary Mean Change from Baseline in Dermatology Life Quality Index (DLQI) Baseline, Week 12
Secondary Pharmacokinetics (PK): Plasma Concentration of LY3972406 Week 12
See also
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