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COMPLETED Phase 2

A Study of Lebrikizumab (LY3650150) in Participants With Moderate-to-Severe Atopic Dermatitis

NCT03443024 · View on ClinicalTrials.gov ↗

Study Summary

The purpose of this study is to evaluate the safety and efficacy of lebrikizumab compared with placebo in participants with moderate-to-severe atopic dermatitis.

Conditions Studied

Interventions

  • DRUG Placebo
  • BIOLOGICAL Lebrikizumab

Study Locations (20)

California

  • Center for Dermatology Clinical Research, Inc. — Fremont
  • University of Southern California — Los Angeles
  • Dermatology Research Associates — Los Angeles
  • Stanford Medicine Outpatient Center-Medical Dermatology Clinic — Redwood City
  • Center for Dermatology and Laser Surgery — Sacramento
  • UCSD Dermatology — San Diego
  • TCR Medical Corporation — San Diego
  • Clinical Science Institute — Santa Monica

Florida

  • Total Vein and Skin — Boynton Beach
  • Florida Academic Centers Research and Education, LLC — Coral Gables
  • Olympian Clinical Research — Largo
  • Tory Sullivan, MD PA — North Miami Beach
  • International Clinical Research - US, LLC — Sanford
  • Integrated Clinical Research, LLC — West Palm Beach

Arkansas

  • Dermatology Trial Associates — Bryant
  • Northwest Arkansas Clinical Trials Center — Rogers

Georgia

  • Marietta Dermatology Clinical Research, Inc. — Marietta
  • Advanced Medical Research, PC — Sandy Springs

Arizona

  • Clear Dermatology & Aesthetics Center — Scottsdale

District of Columbia

  • George Washington Medical Faculty Associates — Washington D.C.

Trial Details

FieldValue
Enrollment Target 280 participants
Start Date 2018-01-30
Est. Completion 2019-05-23
Phase Phase 2

Sponsor

Eli Lilly and Company

704 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT03443024

The ClinicalTrials.gov registry entry for NCT03443024 describes a study currently listed as completed. It is categorized as Phase 2, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 280 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Eli Lilly and Company, which has 704 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 1 condition, with Atopic Dermatitis appearing as the primary indexed condition, and to 2 interventions — of which Placebo is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.

Geographic footprint matters for practical reasons: NCT03443024 reports 20 study locations spanning 6 distinct geographic areas — top geographies include California, Florida, Arkansas. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.

Frequently Asked Questions

What is clinical trial NCT03443024 about?

NCT03443024 is a clinical study titled "A Study of Lebrikizumab (LY3650150) in Participants With Moderate-to-Severe Atopic Dermatitis". The purpose of this study is to evaluate the safety and efficacy of lebrikizumab compared with placebo in participants with moderate-to-severe atopic dermatitis.

What is the current status of trial NCT03443024?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 280 participants. The study started on 2018-01-30. Estimated completion is 2019-05-23.

What conditions does trial NCT03443024 study?

This clinical trial studies the following conditions: Atopic Dermatitis. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT03443024?

The interventions under investigation include: Placebo (DRUG), Lebrikizumab (BIOLOGICAL). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT03443024?

This trial is sponsored by Eli Lilly and Company, which has 704 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT03443024 being conducted?

This trial has 20 study locations across Arizona, Arkansas, California, District of Columbia, Florida. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Related

Data sourced from official U.S. government datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial