Atopic DermatitisPhase 4NCT06116526
Dupilumab De-escalation in Pediatric Atopic Dermatitis
A Phase 4 study testing Dupilumab - Discontinuation, Dupilumab - Dose Reduction and Dupilumab - Standard Dose in people with Atopic Dermatitis, run by Johns Hopkins University at 1 site in United States.
Trial summary
This is a pilot investigator-blinded, randomized clinical trial to assess the feasibility of dupilumab treatment discontinuation or dose-reduction in children aged 1-17 years who have achieved sustained atopic dermatitis (AD) control on dupilumab. Read more about this study
- Who is it for?
- Ages 1 year to 17 years
- Conditions the study is for
- Atopic Dermatitis
- What is being tested?
- Dupilumab - Discontinuation, Dupilumab - Dose Reduction and Dupilumab - Standard Dose
- Type of treatment
- Injection or infusion
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 1 participants
- Where
- 1 siteUnited States
- Study dates
- 1 Apr 2024to 18 Jul 2026
- Phase
- Phase 4
- Are there results?
- None posted in the registry
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 1 year to 17 years
- All sexes
- No healthy volunteers
- Child
Who may be able to join
- Aged 1 to <18 years old, either sex, any race or ethnicity
- Provide signed informed consent by parent or legal guardian and informed assent if applicable
- Has a physician confirmed diagnosis of atopic dermatitis
- Has received dupilumab for at least 12 months for the treatment of atopic dermatitis
- Has had well-controlled atopic dermatitis on dupilumab within last 6 months (defined as POEM<=7, EASI<=7, or IGA<=2)
- Able to speak English
- Able and willing to adhere to all study procedures
Who cannot join
- Taking concurrent systemic medication for atopic dermatitis (e.g., methotrexate, cyclosporine, tralokinumab, abrocitinib, upadacitinib, systemic corticosteroids)
- Using concurrent phototherapy for atopic dermatitis
- Taking dupilumab for a clinical indication other than atopic dermatitis (such as asthma or eosinophilic esophagitis)
- Poor control of atopic dermatitis
- Poor control of asthma or eosinophilic esophagitis
- Has used an investigational drug within 90 days or plan to use an investigational drug during the study period
- Does not have health insurance or will lose health insurance during the study period
Trial locations and contacts
1 site in 1 country.
United States1 site
Johns Hopkins Univerisity
Baltimore, Maryland, 21210
About this study
Official title: Dupilumab De-escalation in Pediatric Atopic Dermatitis: A Pilot Trial
This is a pilot investigator-blinded, randomized clinical trial to assess the feasibility of dupilumab treatment discontinuation or dose-reduction in children aged 1-17 years who have achieved sustained atopic dermatitis (AD) control on dupilumab.
Read the detailed description
Participants will be randomly assigned to one of three groups: discontinuation of dupilumab; reduction of dupilumab dose; or continuation of standard dupilumab dose. During the active study treatment period, participants will be asked to complete 5 study visits. At these visits, a physician will conduct a skin examination to assess atopic dermatitis (AD) severity and participants will complete questionnaires about their AD symptoms and severity. During the observational period, participants will be asked to complete questionnaires about their AD symptoms and medication use every twelve weeks, for a total of 3 follow-up contacts. The purpose of this study is to evaluate the feasibility and sustainability of reducing or discontinuing dupilumab in children with well-controlled AD.
- Conditions
- Atopic Dermatitis
- Being tested
- Dupilumab - Discontinuation, Dupilumab - Dose Reduction, Dupilumab - Standard Dose
- Medical subject headings
- Dermatitis, Atopic
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Dupilumab - DiscontinuationDrug
Also called Dupixent
Drug injections are discontinued.
Dupilumab - Dose ReductionDrug
Also called Dupixent
The drug is given as a subcutaneous injection.
Dupilumab - Standard DoseDrug
Also called Dupixent
The drug is given as a subcutaneous injection.
| Study group | Role | What they receive |
|---|---|---|
| Dupilumab - discontinuation | Experimental | Participants will discontinue their dupilumab treatment for atopic dermatitis. Receives: Drug: Dupilumab - Discontinuation |
| Dupilumab - dose reduction | Experimental | Participants whose standard dupilumab dosing for atopic dermatitis is 200 mg or 300 mg every 2 weeks will decrease drug administration to every 4 weeks, and participants whose standard dupilumab dosing is 200 mg or 300 mg every 4 weeks will decrease administration to every 8 weeks. Receives: Drug: Dupilumab - Dose Reduction |
| Dupilumab - standard dosing | Experimental | Participants will continue to receive standard maintenance dupilumab dosing for atopic dermatitis according to FDA labeling, as indicated below.
Infants ≥6 months and Children <6 years:
5 to <15 kg: 200 mg every 4 weeks. 15 to <30 kg: 300 mg every 4 weeks
Children ≥6 years and Adolescents ≤17 years:
15 to <30 kg: 300 mg every 4 weeks 30 to <60 kg: 200 mg every other week
≥60 kg: 300 mg every other week Receives: Drug: Dupilumab - Standard Dose |
What is being measured
The primary outcome is the main question the study is designed to answer.
Percentage of Participants with Successful Dose Reduction of Dupilumab
Successful de-escalation is defined as maintaining a reduced dose (i.e., less frequent administration) of dupilumab after initial de-escalation on week 0. Patients who require re-escalating the dose of dupilumab to standard dosing or adding other systemic treatments for their AD will be regarded as treatment failure.
Measured: From Baseline through Week 16 (active protocol phase) and Week 17 through Week 52 (observational phase)
Percentage of Participants with Successful Discontinuation of Dupilumab
Successful discontinuation is defined as maintaining discontinuation of dupilumab after initial discontinuation on week 0. Patients who require resumption of dupilumab or beginning other systemic treatments for their AD will be regarded as treatment failure.
Measured: From Baseline through Week 16 (active protocol phase) and Week 17 through Week 52 (observational phase)
Secondary outcomes (14)
Change in Investigator's Global Assessment (IGA) Scores
IGA is a global clinical assessment scale to determine severity of AD and clinical response to treatment on a static 5-point scale (0 = clear; 1 = almost clear; 2 = mild; 3 = moderate; 4 = severe) based on the degree of erythema and papulation/infiltration. The IGA score ranges from 0 to 4. Higher scores indicate greater severity of AD.
Measured: From Baseline through Week 16 (active protocol phase) and Week 17 through Week 52 (observational phase)
Change in Eczema Area and Severity Index (EASI) Scores
The EASI score is used to evaluate severity of AD based on AD clinical signs and % of body surface area (BSA) affected. Severity of clinical signs of AD (erythema, induration/papulation, excoriation and lichenification) scored separately for each of 4 body regions (head and neck, upper limbs, trunk [including axillae and groin] and lower limbs [including buttocks]) on 4-point scale: 0= absent; 1= mild; 2= moderate; 3= severe. The total EASI score ranges from 0 to 72. Higher scores indicate greater severity of AD.
Measured: From Baseline through Week 16 (active protocol phase) and Week 17 through Week 52 (observational phase)
Change in Patient Oriented Eczema Measure (POEM) Scores
The POEM is a 7-item questionnaire to assess disease symptoms in children and adults with AD. It is composed of 7 items (dryness, itching, flaking, cracking, sleep loss, bleeding, and weeping) based on symptom frequency during the past week (0 = 'no days', 1 = '1 to 2 days', 2 = '3 to 4 days', 3 = '5 to 6' days, and 4 = 'every day'). The total POEM score ranges from 0 to 28. Higher scores indicate more severe disease and poor quality of life.
Measured: From Baseline through Week 16 (active protocol phase) and Week 17 through Week 52 (observational phase)
Change in Patient-Reported Outcomes Measurement Information System (PROMIS) Itch questionnaire score
The PROMIS Itch questionnaire measures the extent to which patients experience problems with itchiness over the past 7 days using a 5-point Likert scale (1 = Never; 2 = Rarely; 3 = Sometimes; 4 = Often; and 5 = Almost Always). Higher scores reflect greater severity of experienced itch symptoms.
Measured: From Baseline through Week 16 (active protocol phase) and Week 17 through Week 52 (observational phase)
Change in Patient-Reported Outcomes Measurement Information System (PROMIS) Sleep Problem questionnaire score
The PROMIS Sleep Problem questionnaire measures the extent to which patients experience problems with sleep over the past 7 days using a 5-point Likert scale (1 = Never; 2 = Almost never; 3 = Sometimes; 4 = Almost always; and 5 = Always). The sleep problems contain sleep disturbances (sleep quality, sleep onset, sleep continuity) and sleep-related impairment (perceptions of sleepiness during usual awake hours and reported impairments during the day associated with sleep problems or daytime sleepiness). Higher scores reflect greater severity of sleep problems.
Measured: From Baseline through Week 16 (active protocol phase) and Week 17 through Week 52 (observational phase)
Change in Patient-Reported Outcomes Measurement Information System (PROMIS) Anxiety questionnaire score
The PROMIS Anxiety questionnaire measures the extent to which patients experience problems with anxiety over the past 7 days using a 5-point Likert scale (1 = Never; 2 = Almost never; 3 = Sometimes; 4 = Often; and 5 = Almost Always). The questionnaire includes fear (fearfulness, panic), anxious misery (worry, dread), hyperarousal (tension, nervousness, restlessness), social/separation anxiety (fear or distress when separating from caregivers), and somatic symptoms related to arousal (racing heart, dizziness). Higher scores reflect greater severity of experienced anxiety symptoms.
Measured: From Baseline through Week 16 (active protocol phase) and Week 17 through Week 52 (observational phase)
Change in Patient-Reported Outcomes Measurement Information System (PROMIS) Depressive Symptoms questionnaire score
The PROMIS Depressive Symptoms questionnaire measures the extent to which patients experience problems with depression over the past 7 days using a 5-point Likert scale (1 = Never; 2 = Almost never; 3 = Sometimes; 4 = Almost Always; and 5 = Always). The depressive symptoms include negative mood (sadness, guilt), views of self (self-criticism, worthlessness), and social cognition (loneliness, interpersonal alienation); decreased positive affect, anhedonia (loss of interest, inability to engage in play), and engagement. Higher scores reflect greater severity of experienced depressive symptoms.
Measured: From Baseline through Week 16 (active protocol phase) and Week 17 through Week 52 (observational phase)
Change in Patient-Reported Outcomes Measurement Information System (PROMIS) Cognitive Function questionnaire score
The PROMIS Cognitive Function questionnaire measures the extent to which patients experience problems with cognitive function over the past 4 weeks using a 5-point Likert scale (1 = All of the time; 2 = Most of the time; 3 = Some of the time; 4 = A little of the time; and 5 = None of the time). The questionnaire includes difficulties in cognitive abilities (e.g., memory, attention, and decision making), and difficulties in the application of such abilities to everyday tasks (e.g., planning, organizing, calculating, remembering, and learning). Lower scores reflect greater impact on cognitive function.
Measured: From Baseline through Week 16 (active protocol phase) and Week 17 through Week 52 (observational phase)
Change in Patient-Reported Outcomes Measurement Information System (PROMIS) Global Health questionnaire score
The PROMIS Global Health questionnaire measures the extent to which patients experience problems with global health in general using a 5-point Likert scale (1 = Poor; 2 = Fair; 3 = Good; 4 = Fair; and 5 = Excellent). The questionnaire includes an overall evaluation of physical, mental health, and social health. Higher scores reflect a lower quality of global health.
Measured: From Baseline through Week 16 (active protocol phase) and Week 17 through Week 52 (observational phase)
Change in Patient-Reported Outcomes Measurement Information System (PROMIS) Pain Intensity questionnaire score
The PROMIS Pain Intensity questionnaire measures the intensity of patients' pain due to their AD over the past 7 days using a 10 point scale, with 0 indicating "No Pain" and 10 indicating "the worst pain possible." Higher raw scores reflect greater severity of experienced pain due to AD.
Measured: From Baseline through Week 16 (active protocol phase) and Week 17 through Week 52 (observational phase)
Change in Children's Dermatology Life Quality Index (CDLQI) score
CDLQI is a 10-item questionnaire to assess the impact of skin problems on the quality of life of children between the ages of 4-16 years old over the last one week. Each question is evaluated on a 4-point scale: Not at all = 0, A Little = 1, Quite A Lot = 2, Very Much = 3. Higher scores indicate worse child-reported quality of life. CDLQI scores indicate the degree of severity burden on the quality of life: No effect = 0-1; Small effect = 2-6; Moderate effect = 7-12; Very large effect = 13-18; and Extremely large effect = 19-30.
Measured: From Baseline through Week 16 (active protocol phase) and Week 17 through Week 52 (observational phase)
Change in Family Dermatology Life Quality Index (FDLQI) score
FDLQI is a 10-item questionnaire to assess the impact of skin problems on the quality of life of families over the last one month. Each question is evaluated on a 4-point scale: Not at all = 0, A Little = 1, Quite A Lot = 2, Very Much = 3. Higher scores indicate worse quality of life. FDLQI scores indicate the degree of severity burden on the quality of life: No effect = 0-1; Small effect = 2-6; Moderate effect = 7-12; Very large effect = 13-18; and Extremely large effect = 19-30.
Measured: From Baseline through Week 16 (active protocol phase) and Week 17 through Week 52 (observational phase)
Changes in Utilization of Topical Medications for Atopic Dermatitis
Participants will provide a self-report of their daily utilization of topical medications (medication name, dose and frequency) using a paper-form Daily Diary.
Measured: From Baseline through Week 16 (active protocol phase) and Week 17 through Week 52 (observational phase)
Adverse Events After Dupilumab Dose-reduction or Discontinuation
The number of participants who experience adverse events ≥ Grade 2 is based on the Common Terminology Criteria for Adverse Events (CTCAE). The CTCAE is generally graded as follows: Grade 1 - mild; asymptomatic or mild symptoms; clinical or diagnostic observations only; intervention not needed; Grade 2 - moderate; minimal, local, or noninvasive intervention indicated; limiting age-appropriate instrumental activities of daily living; Grade 3 - severe or medically significant but not immediately life-threatening; hospitalization or prolongation of hospitalization indicated; disabling; limited self care activities of daily living; Grade 4 - life-threatening consequences; urgent intervention indicated; Grade 5 - death related to adverse event.
Measured: From Baseline through Week 16 (active protocol phase) and Week 17 through Week 52 (observational phase)
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted3 Nov 2023
- Study start1 Apr 2024
- Primary completion18 Jul 2026
- Study completion18 Jul 2026
Why it stopped: Poor accrual
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Publications (2)Papers the sponsor has linked to this study.
- Other trials for Atopic DermatitisStudies of the same condition, open and under way.
- More trials run by Johns Hopkins UniversityThe 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 4
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Double blind
- Who is masked
- Investigator, Outcomes assessor
- Enrolment
- 1 participants (actual)
Sponsor and investigators
- Lead sponsor
- Johns Hopkins University
- Sponsor type
- University, hospital or other
- Collaborators
- Doris Duke Charitable Foundation
- Responsible party
- Sponsor
- Investigators
- Joy Wan, MD MSCE, Principal investigator, Johns Hopkins University
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT06116526
- Sponsor's protocol ID
- IRB00405441
- Status last verified
- Nov 2026
- First submitted
- 30 Oct 2023
- Last updated
- 3 Nov 2026
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- Yes
- FDA-regulated device
- No
Publications
Drucker AM, Wang AR, Li WQ, Sevetson E, Block JK, Qureshi AA. The Burden of Atopic Dermatitis: Summary of a Report for the National Eczema Association. J Invest Dermatol. 2017 Jan;137(1):26-30. doi: 10.1016/j.jid.2016.07.012. Epub 2016 Sep 8.
PubMed 27616422Langan SM, Irvine AD, Weidinger S. Atopic dermatitis. Lancet. 2020 Aug 1;396(10247):345-360. doi: 10.1016/S0140-6736(20)31286-1.
PubMed 32738956
Study at a glance
From the registry record, last updated by the sponsor on 3 Nov 2026. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Dupilumab De-escalation in Pediatric Atopic Dermatitis: A Pilot Trial
- ClinicalTrials.gov ID
- NCT06116526
- Acronym / sponsor ID
- IRB00405441
- Conditions
- Atopic Dermatitis
- Phase
- Phase 4
- Study type
- Interventional
- Recruitment status
- TerminatedReason stopped: Poor accrual
- Enrolment
- 1 participants (actual)
- Lead sponsor
- Johns Hopkins UniversityUniversity, hospital or other
- Collaborators
- Doris Duke Charitable Foundation
- Study start
- 1 Apr 2024 (actual)
- Primary completion
- 18 Jul 2026 (actual)
- Study completion
- 18 Jul 2026 (actual)
- First posted
- 3 Nov 2023 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
This is a pilot investigator-blinded, randomized clinical trial to assess the feasibility of dupilumab treatment discontinuation or dose-reduction in children aged 1-17 years who have achieved sustained atopic dermatitis (AD) control on dupilumab.
Detailed description
Participants will be randomly assigned to one of three groups: discontinuation of dupilumab; reduction of dupilumab dose; or continuation of standard dupilumab dose. During the active study treatment period, participants will be asked to complete 5 study visits. At these visits, a physician will conduct a skin examination to assess atopic dermatitis (AD) severity and participants will complete questionnaires about their AD symptoms and severity. During the observational period, participants will be asked to complete questionnaires about their AD symptoms and medication use every twelve weeks, for a total of 3 follow-up contacts. The purpose of this study is to evaluate the feasibility and sustainability of reducing or discontinuing dupilumab in children with well-controlled AD.
Study design
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Double blind (investigator, outcomes assessor)
- Number of arms
- 3
| Arm | Type | Receives |
|---|---|---|
| Dupilumab - discontinuation | Experimental | Drug: Dupilumab - DiscontinuationParticipants will discontinue their dupilumab treatment for atopic dermatitis. |
| Dupilumab - dose reduction | Experimental | Drug: Dupilumab - Dose ReductionParticipants whose standard dupilumab dosing for atopic dermatitis is 200 mg or 300 mg every 2 weeks will decrease drug administration to every 4 weeks, and participants whose standard dupilumab dosing is 200 mg or 300 mg every 4 weeks will decrease administration to every 8 weeks. |
| Dupilumab - standard dosing | Experimental | Drug: Dupilumab - Standard DoseParticipants will continue to receive standard maintenance dupilumab dosing for atopic dermatitis according to FDA labeling, as indicated below. Infants ≥6 months and Children <6 years: 5 to <15 kg: 200 mg every 4 weeks. 15 to <30 kg: 300 mg every 4 weeks Children ≥6 years and Adolescents ≤17 years: 15 to <30 kg: 300 mg every 4 weeks 30 to <60 kg: 200 mg every other week ≥60 kg: 300 mg every other week |
Who may qualify
- Ages
- 1 year to 17 years
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Child
Key inclusion criteria (7 listed)
- Aged 1 to <18 years old, either sex, any race or ethnicity
- Provide signed informed consent by parent or legal guardian and informed assent if applicable
- Has a physician confirmed diagnosis of atopic dermatitis
- Has received dupilumab for at least 12 months for the treatment of atopic dermatitis
- Has had well-controlled atopic dermatitis on dupilumab within last 6 months (defined as POEM<=7, EASI<=7, or IGA<=2)
Key exclusion criteria (7 listed)
- Taking concurrent systemic medication for atopic dermatitis (e.g., methotrexate, cyclosporine, tralokinumab, abrocitinib, upadacitinib, systemic corticosteroids)
- Using concurrent phototherapy for atopic dermatitis
- Taking dupilumab for a clinical indication other than atopic dermatitis (such as asthma or eosinophilic esophagitis)
- Poor control of atopic dermatitis
- Poor control of asthma or eosinophilic esophagitis
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 |
|---|---|---|
| Dupilumab - DiscontinuationAlso: DupixentDrug injections are discontinued. | Drug | Dupilumab - discontinuation |
| Dupilumab - Dose ReductionAlso: DupixentThe drug is given as a subcutaneous injection. | Drug | Dupilumab - dose reduction |
| Dupilumab - Standard DoseAlso: DupixentThe drug is given as a subcutaneous injection. | Drug | Dupilumab - standard dosing |
Primary outcome
Percentage of Participants with Successful Dose Reduction of Dupilumab
Time frame: From Baseline through Week 16 (active protocol phase) and Week 17 through Week 52 (observational phase)
Successful de-escalation is defined as maintaining a reduced dose (i.e., less frequent administration) of dupilumab after initial de-escalation on week 0. Patients who require re-escalating the dose of dupilumab to standard dosing or adding other systemic treatments for their AD will be regarded as treatment failure.
Percentage of Participants with Successful Discontinuation of Dupilumab
Time frame: From Baseline through Week 16 (active protocol phase) and Week 17 through Week 52 (observational phase)
Successful discontinuation is defined as maintaining discontinuation of dupilumab after initial discontinuation on week 0. Patients who require resumption of dupilumab or beginning other systemic treatments for their AD will be regarded as treatment failure.
14 secondary outcomes
Change in Investigator's Global Assessment (IGA) Scores
Time frame: From Baseline through Week 16 (active protocol phase) and Week 17 through Week 52 (observational phase)
Change in Eczema Area and Severity Index (EASI) Scores
Time frame: From Baseline through Week 16 (active protocol phase) and Week 17 through Week 52 (observational phase)
Change in Patient Oriented Eczema Measure (POEM) Scores
Time frame: From Baseline through Week 16 (active protocol phase) and Week 17 through Week 52 (observational phase)
Change in Patient-Reported Outcomes Measurement Information System (PROMIS) Itch questionnaire score
Time frame: From Baseline through Week 16 (active protocol phase) and Week 17 through Week 52 (observational phase)
Change in Patient-Reported Outcomes Measurement Information System (PROMIS) Sleep Problem questionnaire score
Time frame: From Baseline through Week 16 (active protocol phase) and Week 17 through Week 52 (observational phase)
Change in Patient-Reported Outcomes Measurement Information System (PROMIS) Anxiety questionnaire score
Time frame: From Baseline through Week 16 (active protocol phase) and Week 17 through Week 52 (observational phase)
Change in Patient-Reported Outcomes Measurement Information System (PROMIS) Depressive Symptoms questionnaire score
Time frame: From Baseline through Week 16 (active protocol phase) and Week 17 through Week 52 (observational phase)
Change in Patient-Reported Outcomes Measurement Information System (PROMIS) Cognitive Function questionnaire score
Time frame: From Baseline through Week 16 (active protocol phase) and Week 17 through Week 52 (observational phase)
Change in Patient-Reported Outcomes Measurement Information System (PROMIS) Global Health questionnaire score
Time frame: From Baseline through Week 16 (active protocol phase) and Week 17 through Week 52 (observational phase)
Change in Patient-Reported Outcomes Measurement Information System (PROMIS) Pain Intensity questionnaire score
Time frame: From Baseline through Week 16 (active protocol phase) and Week 17 through Week 52 (observational phase)
Change in Children's Dermatology Life Quality Index (CDLQI) score
Time frame: From Baseline through Week 16 (active protocol phase) and Week 17 through Week 52 (observational phase)
Change in Family Dermatology Life Quality Index (FDLQI) score
Time frame: From Baseline through Week 16 (active protocol phase) and Week 17 through Week 52 (observational phase)
Changes in Utilization of Topical Medications for Atopic Dermatitis
Time frame: From Baseline through Week 16 (active protocol phase) and Week 17 through Week 52 (observational phase)
Adverse Events After Dupilumab Dose-reduction or Discontinuation
Time frame: From Baseline through Week 16 (active protocol phase) and Week 17 through Week 52 (observational phase)
Results and safety
The study was stopped early (reason given: Poor accrual). Results are not available in the source record.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 3 Nov 2026.
- Background: PubMed 27616422Drucker AM, Wang AR, Li WQ, Sevetson E, Block JK, Qureshi AA. The Burden of Atopic Dermatitis: Summary of a Report for the National Eczema Association. J Invest Dermatol. 2017 Jan;137(1):26-30. doi: 10.1016/j.jid.2016.07.012. Epub 2016 Sep 8.
- Background: PubMed 32738956Langan SM, Irvine AD, Weidinger S. Atopic dermatitis. Lancet. 2020 Aug 1;396(10247):345-360. doi: 10.1016/S0140-6736(20)31286-1.
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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.
Joy Wan, MD MSCE principal investigator
Johns Hopkins University
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A Phase 4 study testing Dupilumab - Discontinuation, Dupilumab - Dose Reduction and Dupilumab - Standard Dose in people with Atopic Dermatitis, run by Johns Hopkins University at 1 site in United States.
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 7 inclusion and 7 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 3 Nov 2026. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in United States. 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. 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 4 studies take place after a treatment is approved, to learn more about its long-term benefits and risks in everyday use.
Not every study follows the same path, and some studies (observational studies, device studies) have no phase.
Are results available for this study?
The study was stopped early (reason given: Poor accrual). Results are not available in the source record.
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 with Successful Dose Reduction of Dupilumab (time frame: From Baseline through Week 16 (active protocol phase) and Week 17 through Week 52 (observational phase)). The study lists 2 primary outcomes in all. It is what the study was designed to measure, not a finding.
Where can I read the original study information?
On the ClinicalTrials.gov record for NCT06116526, which also lists 2 linked publications.
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 3 Nov 2026.