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Completed Phase 3 Interventional

A Study to Investigate the Efficacy and Safety of Lebrikizumab in Participants With Moderate-to-Severe Atopic Hand and Foot Dermatitis

ClinicalTrials.gov ID: NCT06921759

Public ClinicalTrials.gov record NCT06921759. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 21, 2026, 9:10 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Multicenter, Randomized, Double-Blind, Placebo-Controlled, Parallel-Group Study to Evaluate the Efficacy and Safety of Lebrikizumab in Adult and Adolescent Participants With Moderate-to-Severe Atopic Hand and Foot Dermatitis

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

The main purpose of this study is to assess the efficacy of lebrikizumab versus placebo on skin lesions in adults and adolescent participants with atopic hand and foot dermatitis. This study lasts up to 32 weeks, including a 6-week screening period, a 16-week treatment period, and a safety follow-up visit 12 weeks after the last dose.

Study identification

NCT ID
NCT06921759
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Eli Lilly and Company
Industry
Enrollment
221 participants

Conditions and interventions

Interventions

Drug

Eligibility (public fields only)

Age range
12 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Apr 21, 2025 (Actual)
Primary completion
May 13, 2026 (Actual)
Completion
Jul 28, 2026 (Actual)
Last update posted
Aug 20, 2026

2025 – 2026

United States locations

U.S. sites
14
U.S. states
9
U.S. cities
13
Facility City State ZIP Site status
First OC Dermatology Research Inc Fountain Valley California 92708 —
Dermatology Research Associates Los Angeles California 90045 —
Encore Medical Research Hollywood Florida 33024 —
Research Associates of South Florida - Miami - Southwest 8th Street Miami Florida 33134 —
Renstar Medical Research Ocala Florida 34470 —
DeNova Research Chicago Illinois 60602 —
Southern Indiana Clinical Trials New Albany Indiana 47150 —
Revival Research Institute, LLC Troy Michigan 48084 —
MediSearch Clinical Trials Saint Joseph Missouri 64506 —
Care Access - Hoboken Hoboken New Jersey 07030 —
Optima Research - Boardman Boardman Ohio 44512 —
Progressive Clinical Research San Antonio Texas 78213 —
Texas Dermatology and Laser Specialists San Antonio Texas 78218 —
Complete Dermatology Sugar Land Texas 77479 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 62 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT06921759, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Aug 20, 2026 · Synced Oct 21, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT06921759 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →