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.
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
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
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
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
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
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
Austria3 sites
LKH Feldkirch
Feldkirch, Vorarlberg, 6807
Universitätsklinikum Graz
Graz, Styria, 8036
Sozialmed. Zentrum Ost - Donauspital
Vienna, 1220
Italy3 sites
Polic.Umberto I -Univ. La Sapienza
Roma, 00161
Policlinico di Tor Vergata
Rome, Lazio, 00133
Istituto Clinico Humanitas
Rozzano, Milano, 20089
Czechia2 sites
Clintrial, s.r.o.
Prague, Hl. M. Praha, 100 00
Sanatorium Profesora Arenbergera
Prague, 110 00
Germany2 sites
Dermatologikum Hamburg
Hamburg, 20354
TFS Trial Form Support GmbH
Hamburg, 20537
Mexico2 sites
Derma Norte del Bajío, S.C.
Aguascalientes
Grupo Medico Camino S.C.
Mexico City, Mexico City, 03310
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).
- Conditions
- Atopic Dermatitis
- 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 group | Role | What they receive |
|---|---|---|
| 50 mg LY3375880 | Experimental | Induction Period:
Participants received 50 mg LY3375880 administered SC Q4W. Receives: Drug: LY3375880 |
| 150 mg LY3375880 | Experimental | Induction Period:
Participants received 150 mg LY3375880 administered SC Q4W. Receives: Drug: LY3375880 |
| 600 mg LY3375880 | Experimental | Induction Period:
Participants received 600 mg LY3375880 administered SC Q4W. Receives: Drug: LY3375880 |
| Placebo | Placebo comparator | Induction 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.
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)
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
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
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
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
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
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
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.
- First posted5 Feb 2019
- Study start12 Feb 2019
- Primary completion27 Feb 2020
- Study completion27 Feb 2020
Why it stopped: The study was terminated for lack of efficacy after an interim analysis was performed
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Posted resultsParticipant flow, outcome measures and adverse events reported by the sponsor.
- Other trials for Atopic DermatitisStudies of the same condition, open and under way.
- More trials run by Eli Lilly and CompanyThe sponsor's other registered studies.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
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)
Sponsor and investigators
- Lead sponsor
- Eli Lilly and Company
- Sponsor type
- Industry (pharma, biotech, devices)
- Responsible party
- Sponsor
- Investigators
- Call 1-877-CTLILLY (1-877-285-4559) or 1-317-615-4559 Mon - Fri 9 AM - 5 PM Eastern time (UTC/GMT - 5 hours, EST), Study director, Eli Lilly and Company
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
- Results posted
- Yes, on ClinicalTrials.gov
- 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.
Study at a glance
From the registry record, last updated by the sponsor on 20 Apr 2021. Recruitment status is as the sponsor reported it: confirm with the study team.
- 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
- ClinicalTrials.gov ID
- NCT03831191
- Acronym / sponsor ID
- ADmIRe / 17104
- Conditions
- Atopic Dermatitis
- Keywords
- eczema, atopic eczema
- Phase
- Phase 2
- Study type
- Interventional
- Recruitment status
- TerminatedReason stopped: The study was terminated for lack of efficacy after an interim analysis was performed
- Enrolment
- 136 participants (actual)
- Lead sponsor
- Eli Lilly and CompanyIndustry (pharma, biotech, devices)
- Study start
- 12 Feb 2019 (actual)
- Primary completion
- 27 Feb 2020 (actual)
- Study completion
- 27 Feb 2020 (actual)
- First posted
- 5 Feb 2019 (actual)
- Results
- Posted 20 Apr 2021
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
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).
Study design
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Double blind (participant, investigator)
- Number of arms
- 4
| Arm | Type | Receives |
|---|---|---|
| 50 mg LY3375880 | Experimental | Drug: LY3375880Induction Period: Participants received 50 mg LY3375880 administered SC Q4W. |
| 150 mg LY3375880 | Experimental | Drug: LY3375880Induction Period: Participants received 150 mg LY3375880 administered SC Q4W. |
| 600 mg LY3375880 | Experimental | Drug: LY3375880Induction Period: Participants received 600 mg LY3375880 administered SC Q4W. |
| Placebo | Placebo comparator | Drug: PlaceboInduction Period: Participants received placebo administered subcutaneously (SC) every 4 weeks (Q4W). |
Who may qualify
- Ages
- 18 years and older
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
Key inclusion criteria (3 listed)
- 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).
Key exclusion criteria (1 listed)
- Participants must not have concurrent treatment with topical or systemic treatments for AD.
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| LY3375880Administered SC | Drug | 150 mg LY3375880, 50 mg LY3375880, 600 mg LY3375880 |
| PlaceboAdministered SC | Drug | Placebo |
Primary outcome
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
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.
7 secondary outcomes
Percentage of Participants Achieving Eczema Area and Severity Index 75 (EASI-75)
Time frame: Week 16
Percentage of Participants Achieving SCORing Atopic Dermatitis 75 (SCORAD-75)
Time frame: Week 16
Percentage of Participants Achieving vIGA-AD of 0
Time frame: Week 16
Mean Change From Baseline in Eczema Area and Severity Index (EASI) Score
Time frame: Baseline, Week 16
Mean Change From Baseline in SCORAD
Time frame: Baseline, Week 16
Percentage of Participants Achieving vIGA-AD of 0 or 1 With a >=2-point Improvement at Week 52
Time frame: Week 52
Pharmacokinetics (PK): Area Under the Concentration Versus Time Curve at a Steady State (AUCτ,ss) of LY3375880
Time frame: 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
Results and safety
Loading the posted results from ClinicalTrials.gov…
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 20 Apr 2021.
- Posted resultsParticipant flow, baseline, all outcome measures and adverse events.
- A Study of LY3375880 in Adults With Moderate-to-Severe Atopic DermatitisLink provided by the sponsor.
- Individual participant dataSharing planned: 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.
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
Call 1-877-CTLILLY (1-877-285-4559) or 1-317-615-4559 Mon - Fri 9 AM - 5 PM Eastern time (UTC/GMT - 5 hours, EST) study director
Eli Lilly and Company
58 sites in 13 countries: see every site and its status.
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.