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A Study of LY4005130 in Adult Participants With Severe Alopecia Areata (Hair Loss)

RecruitingPhase 2

A Phase 2, Randomized, Multicenter, Double-Blind, Placebo-Controlled Proof of Concept Study to Investigate Efficacy and Safety of LY4005130 in Adult Participants With Severe Alopecia Areata

Who can join

Ages 18 to 50 · All sexes

Full eligibility criteria
Inclusion Criteria:

* Have severe Alopecia Areata (AA) that meets all of the following criteria:

  * Hair loss encompassing ≥50% and ≤90% of the scalp, as measured by Severity of Alopecia Tool (SALT) score
  * The duration of the current episode of severe AA is at least 6 months and does not exceed 4 years
  * No significant spontaneous hair regrowth in the investigator's opinion for at least 6 months
  * Agree not to use any AA treatments during the study

Exclusion Criteria:

* Primarily "diffuse" type of AA (characterized by diffuse hair shedding)
* Are currently experiencing other forms of alopecia
* Participants who, in the opinion of the investigator, are currently experiencing or have a history of unstable concomitant disease that requires frequent hospitalizations, and/or frequent use of systemic immunosuppressants that may interfere with participation in the study
* Have received oral JAK Inhibitors in the past
* Have had any major surgery within 8 weeks prior to screening or will require major surgery during the study
* Have a history or presence of cardiovascular, respiratory, hepatic, gastrointestinal, endocrine, hematological, neurological, or neuropsychiatric disorders or any other serious and/or unstable illness

About the study

The purpose of this study is to evaluate how well LY4005130 works in participants with severe alopecia areata (hair loss) when compared with placebo, and how well it's tolerated and what side effects may occur. Blood tests will be performed to investigate how the body processes the study drug and how the study drug affects the body.

The study drug will be administered intravenously (IV) (into a vein in the arm).

The study will last approximately 48 weeks, including screening.

What is being tested

Sponsor: Eli Lilly and Company · Participants: 60 · Started: Apr 14, 2026

Contact the study team

Official record on ClinicalTrials.gov — NCT07533006

Locations in the U.S.

CaliforniaCenter For Dermatology Clinical Research, Inc., Fremont
Northridge Clinical Trials, Northridge
Cura Clinical Research - Santa Clarita - Kelly Johnson Parkway, Santa Clarita
FloridaHealth Clinical Research, LLC, Cutler Bay
MassachusettsBrigham and Women's Hospital, Boston
MichiganRevival Research Institute, LLC, Troy
New HampshireStracskin, Portsmouth
TexasTexas Dermatology and Laser Specialists - San Antonio - South New Braunfels Avenue, San Antonio
UtahJordan Valley Dermatology & Research Center, South Jordan

Conditions

From ClinicalTrials.gov, data retrieved Oct 2, 2026. Each study sets its own eligibility; the study team decides who can join.