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Atopic DermatitisPhase 2ADmIReNCT03831191

A Study of LY3375880 in Adults With Moderate-to-Severe Atopic Dermatitis

A Phase 2 study testing LY3375880 in people with Atopic Dermatitis, run by Eli Lilly and Company at 58 sites in 13 countries.

Terminated

Stopped early. The study ended before it was planned to and will not resume.

Official record
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Trial summary

The reason for this study is to see if the study drug LY3375880 is safe and effective in adults with moderate-to-severe atopic dermatitis (AD). Read more about this study

Who is it for?
Ages 18 years and older
Conditions the study is for
Atopic Dermatitis
What is being tested?
LY3375880
Type of treatment
Injection or infusion
Could I receive a placebo?
Yes, some participants may receive a placebo
How many people
136 participants
Where
58 sitesin 13 countries
Study dates
12 Feb 2019to 27 Feb 2020
Phase
Phase 2
Are there results?
Yes, posted in the registrySummary in the doctors' view

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 years and older
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Who may be able to join

  • Participants must have diagnosis of AD >= 12 months according to the American Academy of Dermatology criteria.
  • Participants must have moderate to severe AD at screening and randomization.
  • Participants must have inadequate response to topical medications within 6 months of screening (or history of intolerance).

Who cannot join

  • Participants must not have concurrent treatment with topical or systemic treatments for AD.

Trial locations and contacts

58 sites in 13 countries.

58 sites in 13 countries

United States14 sites
  • Piedmont Plastic Surgery and Dermatology

    Charlotte, North Carolina, 28277

  • Tien Q. Nguyen, MD inc. DBA First OC Dermatology

    Fountain Valley, California, 92708

  • Center for Clinical Studies

    Houston, Texas, 77004

  • Clinical Partners LLC

    Johnston, Rhode Island, 02919

  • Dermatology Research Associates

    Los Angeles, California, 90045

  • Hightower Clinical Trial Services

    Norman, Oklahoma, 73072

  • Quest Dermatology Research

    Northridge, California, 91324

  • Oregon Dermatology and Research Center

    Portland, Oregon, 97210

  • ActivMed Practices & Research, Inc

    Portsmouth, New Hampshire, 03801

  • Dermatology and Skin Cancer Specialists

    Rockville, Maryland, 20850

  • Arlington Dermatology

    Rolling Meadows, Illinois, 60008

  • Integrative Skin Science and Research

    Sacramento, California, 95815

  • The South Bend Clinic

    South Bend, Indiana, 46617

  • PMG Research of Wilmington, LLC

    Wilmington, North Carolina, 28411

Other trials in United States

Japan10 sites
  • Yasumoto Dermatology Clinic

    Chikushino-shi, Fukuoka, 818 0083

  • Sumire Dermatology Clinic

    Edogawa-ku, Tokyo, 133-0057

  • Matsuda Tomoko Dematological Clinic

    Fukuoka, 819 0167

  • Kobe University Hospital

    Kobe, Hyōgo, 650-0017

  • Dokkyo Medical University Saitama Medical Center

    Koshigaya, Saitama, 343 8555

  • Kyoto Prefectural University of Medicine

    Kyoto, Kyoto, 602-8566

  • Kume Clinic

    Nishi-ku Sakai-shi, Osaka, 593-8324

  • Meiwa Hospital

    Nishinomiya, Hyōgo, 663-8186

  • Takagi Dermatological Clinic

    Obihiro, Hokkaido, 080-0013

  • Oita University Hospital

    Yufu-shi, Oita Prefecture, 8795593

Other trials in Japan

Argentina7 sites
  • Centro de Investigaciones Metabólicas (CINME)

    Buenos Aires, C1027AAP

  • DOM- Centro de Reumatologia

    CABA, Buenos Aires, 1111

  • Buenos Aires Skin

    Ciudad Autonoma Buenos Aires, C1055AA0

  • Instituto de Neumonología y Dermatología

    Ciudad Autonoma Buenos Aires, C1425BEA

  • Psoriahue Medicina Interdisciplinaria

    Ciudad Autonoma Buenos Aires, C1425DKG

  • Parra Dermatología

    Mendoza, 5500

  • Centro Medico Privado de Reumatologia

    San Miguel de Tucumán, T4000AXL

Other trials in Argentina

Puerto Rico5 sites
  • Office of Dr. Samuel Sanchez PSC

    Caguas, PR, 00727

  • Office of Dr. Alma M. Cruz

    Carolina, PR, 00985

  • Ponce School of Medicine CAIMED Center

    Ponce, PR, 00716

  • GCM Medical Group PSC

    San Juan, PR, 00917

  • Clinical Research Puerto Rico, Inc.

    San Juan, 00909

Other trials in Puerto Rico

Hungary4 sites
  • UNO Medical Trials Kft.

    Budapest, 1135

  • Oroshaza Varosi Onkormanyzat Korhaza

    Orosháza, Bekes County, 5900-H

  • Allergo-Derm Bakos Kft

    Szolnok, Jász-Nagykun-Szolnok, 5000

  • MedMare Bt

    Veszprém, 8200

Other trials in Hungary

Spain4 sites
  • Hospital Universitari de Bellvitge

    L'Hospitalet de Llobregat, Barcelona, 08907

  • Clinica Universidad De Navarra

    Madrid, 28027

  • Hospital Universitario La Paz

    Madrid, 28046

  • Clinica Universitaria De Navarra

    Pamplona, Navarre, 31008

Other trials in Spain

Austria3 sites
  • LKH Feldkirch

    Feldkirch, Vorarlberg, 6807

  • Universitätsklinikum Graz

    Graz, Styria, 8036

  • Sozialmed. Zentrum Ost - Donauspital

    Vienna, 1220

Other trials in Austria

Italy3 sites
  • Polic.Umberto I -Univ. La Sapienza

    Roma, 00161

  • Policlinico di Tor Vergata

    Rome, Lazio, 00133

  • Istituto Clinico Humanitas

    Rozzano, Milano, 20089

Other trials in Italy

Czechia2 sites
  • Clintrial, s.r.o.

    Prague, Hl. M. Praha, 100 00

  • Sanatorium Profesora Arenbergera

    Prague, 110 00

Other trials in Czechia

Germany2 sites
  • Dermatologikum Hamburg

    Hamburg, 20354

  • TFS Trial Form Support GmbH

    Hamburg, 20537

Other trials in Germany

Mexico2 sites
  • Derma Norte del Bajío, S.C.

    Aguascalientes

  • Grupo Medico Camino S.C.

    Mexico City, Mexico City, 03310

Other trials in Mexico

Canada1 site
  • The Guenther Dermatology Research Centre

    London, Ontario, N6A 3H7

Other trials in Canada

France1 site
  • CHU de Nice Hopital de L'Archet

    Nice, 06202

Other trials in France

About this study

Official title: A Multicenter, Randomized, Double-Blind, Placebo-Controlled, Phase 2 Study to Evaluate the Efficacy and Safety of LY3375880 in Adult Subjects With Moderate-to-Severe Atopic Dermatitis: The ADmIRe Study

The reason for this study is to see if the study drug LY3375880 is safe and effective in adults with moderate-to-severe atopic dermatitis (AD).

Being tested
LY3375880, Placebo
Keywords
eczema, atopic eczema
Medical subject headings
Dermatitis, Atopic, Eczema

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • LY3375880Drug

    Administered SC

  • PlaceboDrug

    Administered SC

Study groups in NCT03831191
Study groupRoleWhat they receive
50 mg LY3375880ExperimentalInduction Period: Participants received 50 mg LY3375880 administered SC Q4W.
Receives: Drug: LY3375880
150 mg LY3375880ExperimentalInduction Period: Participants received 150 mg LY3375880 administered SC Q4W.
Receives: Drug: LY3375880
600 mg LY3375880ExperimentalInduction Period: Participants received 600 mg LY3375880 administered SC Q4W.
Receives: Drug: LY3375880
PlaceboPlacebo comparatorInduction Period: Participants received placebo administered subcutaneously (SC) every 4 weeks (Q4W).
Receives: Drug: Placebo

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Percentage of Participants Achieving Validated Investigator's Global Assessment for AD (vIGA-AD) of 0 or 1 With a ≥2 Point Improvement

    vIGA-AD measures participants' overall severity of their atopic dermatitis (AD), based on a static, numeric 5 point scale from 0 (clear) to 4 (severe). Higher scores indicate greater severity.The score is based on an overall assessment of the degree of erythema, papulation/induration, oozing/crusting, and lichenification. Non-responder imputation (NRI) method was used to impute missing data.

    Measured: Week 16

Secondary outcomes (7)
  1. Percentage of Participants Achieving Eczema Area and Severity Index 75 (EASI-75)

    EASI assesses objective physician estimates of 2 dimensions of atopic dermatitis - disease extent and clinical signs - by scoring the extent of disease (percentage of skin affected: 0 = 0%; 1 = 1-9%; 2 = 10-29%; 3 = 30-49%; 4 = 50-69%; 5 = 70-89%; 6 = 90-100%) and the severity of 4 clinical signs (erythema, edema/papulation, excoriation, and lichenification) each on a scale of 0 to 3 (0 = none, absent; 1 = mild; 2 = moderate; 3 = severe) at 4 body sites (head and neck, trunk, upper limbs, and lower limbs). Half scores are allowed. Each body site will have a score that ranges from 0 to 72, and the final EASI score will be obtained by weight-averaging these 4 scores. Hence, the final EASI score will range from 0 to 72 (severe) for each time point. A higher score represented greater disease severity.The EASI75 is defined as a ≥ 75% improvement from baseline in the EASI score. Non-responder imputation (NRI) method was used to impute missing data.

    Measured: Week 16

  2. Percentage of Participants Achieving SCORing Atopic Dermatitis 75 (SCORAD-75)

    The SCORAD index uses the rule of nines to assess disease extent (head and neck 9%; upper limbs 9% each; lower limbs 18% each; anterior trunk 18%; back 18%; and genitals 1%). It evaluates 6 clinical characteristics to determine disease severity: (1) erythema, (2) edema/papulation, (3) oozing/crusts, (4) excoriation, (5) lichenification, and (6) dryness on a scale of 0 to 3 (0=absence, 1=mild, 2=moderate, 3=severe). The SCORAD index also assesses subjective symptoms of pruritus and sleep loss in the last 72 hours on visual analogue scales (VAS) of 0 to 10 where 0 is no itch or sleep loss and 10 is worst imaginable itch or sleep loss. These 3 aspects: extent of disease, disease severity, and subjective symptoms combine to give a score between 0(no disease) and 103 (severe disease). Higher scores indicate greater severity.Non-responder imputation (NRI) method was used to impute missing data.

    Measured: Week 16

  3. Percentage of Participants Achieving vIGA-AD of 0

    vIGA-AD measures participants overall severity of their atopic dermatitis (AD), based on a static, numeric 5 point scale from 0 (clear) to 4 (severe). Higher scores indicate greater severity. The score is based on an overall assessment of the degree of erythema, papulation/induration, oozing/crusting, and lichenification. Non-responder imputation (NRI) method was used to impute missing data.

    Measured: Week 16

  4. Mean Change From Baseline in Eczema Area and Severity Index (EASI) Score

    EASI assesses objective physician estimates of 2 dimensions of atopic dermatitis-disease extent and clinical signs-by scoring the extent of disease(percentage of skin affected: 0= 0%;1 =1-9%; 2 =10-29%;3 = 30-49%;4 = 50-69%;5 = 70-89%;6 = 90-100%) and the severity of 4 clinical signs (erythema,edema/papulation,excoriation,and lichenification) each on a scale of 0 to 3 (0 = none, absent; 1 =mild; 2 = moderate; 3=severe) at 4 body sites(head and neck,trunk,upper limbs,and lower limbs).Half scores are allowed.Each body site will have a score that ranges from 0 to 72,and the final EASI score will be obtained by weight-averaging these 4 scores.Hence,the final EASI score will range from 0 to 72(severe) for each time point.Higher scores indicate greater severity.Least Squares Mean(LS Means) were calculated using mixed model repeated measures(MMRM) with treatment,region, baseline disease severity,visit,treatment-by-visit-interaction,baseline and baseline-by-visit-interaction as fixed effects.

    Measured: Baseline, Week 16

  5. Mean Change From Baseline in SCORAD

    The SCORAD index uses the rule of nines to assess disease extent (head and neck 9%;upper limbs 9% each;lower limbs 18% each;anterior trunk 18%;back 18%;and genitals 1%).It evaluates 6 clinical characteristics to determine disease severity: (1)erythema,(2)edema/papulation, (3)oozing/crusts,(4) excoriation,(5) lichenification, and (6) dryness on a scale of 0 to 3(0=absence,1=mild,2=moderate,3=severe).The SCORAD index also assesses subjective symptoms of pruritus and sleep loss in the last 72 hours on visual analogue scales(VAS) of 0 to 10 where 0 is no itch or sleep loss and 10 is worst imaginable itch or sleep loss.These 3 aspects: extent of disease,disease severity,and subjective symptoms combine to give a score between 0(no disease) and 103(severe disease).Higher scores indicate greater severity. LS Means were calculated using a MMRM model with treatment,region,baseline disease severity,visit, treatment-by-visit-interaction,baseline and baseline-by-visit-interaction as fixed effects.

    Measured: Baseline, Week 16

  6. Percentage of Participants Achieving vIGA-AD of 0 or 1 With a >=2-point Improvement at Week 52

    vIGA-AD measures participants overall severity of their atopic dermatitis (AD), based on a static, numeric 5 point scale from 0 (clear) to 4 (severe). Higher scores indicate greater severity. The score is based on an overall assessment of the degree of erythema, papulation/induration, oozing/crusting, and lichenification. Non-responder imputation (NRI) method was used to impute missing data.

    Measured: Week 52

  7. Pharmacokinetics (PK): Area Under the Concentration Versus Time Curve at a Steady State (AUCτ,ss) of LY3375880

    Pharmacokinetics (PK): Area Under the Concentration Versus Time Curve at a steady state (AUCτ,ss) of LY3375880. The PK model was fit using all quantifiable concentrations that were collected in the study (i.e., from the induction and maintenance periods).

    Measured: Induction Period: Pre-dose, Day 0, Day 7, Day 14, Day 28, Day 56, Day 112 Post-dose; Maintenance Period:Predose, Day 168; Day 252, Day 364 Post-dose

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted5 Feb 2019
  2. Study start12 Feb 2019
  3. Primary completion27 Feb 2020
  4. Study completion27 Feb 2020

Why it stopped: The study was terminated for lack of efficacy after an interim analysis was performed

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase 2
Primary purpose
Treatment
Allocation
Randomised
Intervention model
Parallel groups
Masking
Double blind
Who is masked
Participant, Investigator
Enrolment
136 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT03831191
Sponsor's protocol ID
17104
Other IDs
I9N-MC-FCAB, 2018-002401-56, 2018
Acronym
ADmIRe
Status last verified
Jun 2020
First submitted
4 Feb 2019
Last updated
20 Apr 2021
Data monitoring committee
No
FDA-regulated drug
Yes
FDA-regulated device
No
Individual data sharing
Yes: Anonymized individual patient level data will be provided in a secure access environment upon approval of a research proposal and a signed data sharing agreement.

Questions about this trial

What is this clinical trial studying?

A Phase 2 study testing LY3375880 in people with Atopic Dermatitis, run by Eli Lilly and Company at 58 sites in 13 countries.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 3 inclusion and 1 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: stopped early, as of the sponsor's last update on 20 Apr 2021. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 58 sites in United States, Japan, Argentina, Puerto Rico, Hungary and 8 more countries. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. Some participants in this study may receive a placebo. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

What does this phase mean?

Phase 2 studies give the treatment to a larger group to see whether it has the intended effect and to keep checking safety.

Not every study follows the same path, and some studies (observational studies, device studies) have no phase.

Are results available for this study?

Yes. Results are posted in the registry (first posted 20 Apr 2021). A summary is in the For doctors view, and the full results are on ClinicalTrials.gov.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Percentage of Participants Achieving Validated Investigator's Global Assessment for AD (vIGA-AD) of 0 or 1 With a ≥2 Point Improvement (time frame: Week 16). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 20 Apr 2021.

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