NCT05486208TerminatedPhase 1
A Study of LY3844583 in Healthy Participants and Participants With Atopic Dermatitis
A Phase 1, Multicenter, Randomized, Placebo-Controlled, Double-Blind, Single-Ascending Dose Study of LY3844583 in Healthy Participants, and Multiple-Dose Study of LY3844583 in Healthy Participants and Patients With Atopic Dermatitis
Source: ClinicalTrials.gov · Last updated 13 Oct 2026
Reason given: Study terminated due to lack of efficacy signal in atopic dermatitis participants.
Brief summary (registry, in English)
The main purpose of this study is to evaluate the safety and tolerability of LY3844583 in healthy participants and participants with atopic dermatitis (AtD). The study will also assess how fast LY3844583 gets into the blood stream and how long it takes the body to remove it. The study is open to healthy participants and participants with atopic dermatitis. The study will be conducted in three parts and each participant will enroll in one part. The study will last up to 85, 113, and 183 days with 10, 18, and 14 visits for each participant in parts A, B, and C, respectively.
- Status (registry)
- Terminated
- Phase (registry)
- Phase 1
- Study type
- Interventional
- Enrollment
- 86 (actual)
- First submitted
- 2 Aug 2022
- Start date
- 11 Aug 2022
- Primary completion date
- 20 Jan 2024
- Lead sponsor
- Eli Lilly and Company
- Diseases
- Atopic dermatitis (eczema)
- NCT number
- NCT05486208
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Prior treatment
- Atopic dermatitis participants:
- Must not have received certain topical medications for AtD within 2 weeks prior to randomization
- Must not have received certain oral medications for AtD or received phototherapy within 4 weeks prior to randomization
- Must not have received any antibody-based biologic agents (marketed or investigational) within 5 half lives (t1/2) of the drug prior to randomization
- Must not have received intravenous, intramuscular, or intra-articular steroids in the past 6 weeks prior to randomization
Lab values
- All participants:
- Have or used to have health problems or laboratory test results or electrocardiogram (ECG) readings that, in the opinion of the doctor, could make it unsafe to participate, or could interfere with understanding the results of the study
- Have active or latent tuberculosis
- Have had any cancer within the past 5 years. Exceptions: successfully treated basal cell skin carcinoma or squamous cell skin carcinoma, with no evidence of recurrence or metastatic disease within the 3 years prior to baseline
- Have one of the following viral infections: hepatitis B virus, hepatitis C virus or human immunodeficiency virus.
- Have received treatment with biologic agents (such as monoclonal antibodies, including marketed drugs) within 30 days or 5 half-lives (whichever is longer) prior to dosing
- Must not have previously completed a clinical trial with a molecule targeting interleukin-33 and/or the interleukin-33 receptor (ST2)
- Are currently participating in or completed a clinical trial within the last 30 days
- Have received a vaccine containing a live (attenuated) virus within 28 days of screening or intend to receive during the course of the study
Who the study is looking for
- Healthy participants (Parts A and B):
- Are male or female not of childbearing potential
- Inclusion of healthy Japanese participants, the participant must be first-generation Japanese, defined as the participant's biological parents and all of the participant's biological grandparents must be of exclusive Japanese descent, and must have been born in Japan.
- Inclusion of healthy Chinese participants, the participant must be at a minimum, third-generation Chinese, defined as all 4 of the participants' biological grandparents must be of exclusive Chinese descent and born in China.
- Must have a body mass index of 18.0 to 32.0 kilograms per meter squared (kg/m²), inclusive. For healthy Japanese participants, have a body mass index of 18.0 to 28.0 kg/m², inclusive, and a body weight of 50 kg to 85 kg, inclusive.
- Atopic dermatitis participants (Part C):
- Must have a body mass index of 18.0 to 45.0 kg/m², inclusive
- Are male or female participants including those of child bearing potential
- Must have a diagnosis of AtD for at least 12 months with either poor response to topical treatments or inability to use topical treatments
- Must agree to use moisturizer daily throughout the treatment period
Age in the registry: 18 years to 65 years · Sex: All · Accepts healthy volunteers
Sites (3)
Sites in registry order. Save your city in your profile to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| P-One Clinic | Hachiōji | Japan | Unknown status |
| Medical Corporation Heishinkai OPHAC Hospital | Osaka | Japan | Unknown status |
| Parexel Early Phase Unit at Glendale | Glendale | United States | Unknown status |
This page is information, not medical advice. Discuss any trial with your doctor.