Tests eblasakimab in adults with moderate-to-severe atopic dermatitis who previously used dupilumab
Tests eblasakimab against placebo in adults with moderate-to-severe atopic dermatitis previously treated with dupilumab.
Plain-language title generated from the registry record
Registry title: A Randomized, Double-Blind, Placebo-Controlled, Multicenter Trial to Evaluate the Efficacy and Safety of Eblasakimab in Male or Female Moderate-to-Severe Atopic Dermatitis Patients Previously Treated with Dupilumab.
Key facts
- Where
- Berlin, Buxtehude, and Hamburg, GermanySee the 3 sites
- Phase
- Phase 2
Where in Germany
- Charite Universitaetsmedizin Berlin KöRBerlin, GermanyNot yet recruiting
- Elbe Kliniken Stade-Buxtehude Elbe Klinikum Buxtehude gGmbHBuxtehude, GermanyNot yet recruiting
- TFS Trial Form Support GmbHHamburg, GermanyNot yet recruiting
Questions to ask the study team
- How often do I need to come in, and for how long each time?
- Are travel costs paid?
- Can I keep my own doctor?
- What happens if I want to stop?
Trial details
- Who runs it
- Aslan Pharmaceuticals Pte Ltd
- Trial code
- NCT05694884EU 2023-508329-28-00
- Record updated
- 31 May 2024
- Original description
To evaluate the efficacy of eblasakimab in participants with moderate-to severe AD previously treated with dupilumab.Read full original descriptionShow less
A Randomized, Double-Blind, Placebo-Controlled, Multicenter Trial to Evaluate the Efficacy and Safety of Eblasakimab in Male or Female Moderate-to-Severe Atopic Dermatitis Patients Previously Treated with Dupilumab.
To evaluate the efficacy of eblasakimab in participants with moderate-to severe AD previously treated with dupilumab.
Inclusion: Male or female participants ≥18 years old; Willing and able to comply with clinic visits and study-related procedures; Chronic AD present for at least 1 year prior to the Screening visit; Have a vIGA score of ≥3 (5-point scale, 0-4) at the Baseline; Have ≥10% BSA of AD involvement at the Baseline; Have an EASI score ≥18 at the Screening and Baseline visits; History of inadequate response to, intolerance to or contraindication to a stable regimen of topical corticosteroids (TCS) or topical calcineurin inhibitors (TCI) as treatment for AD; All participants must have previously been treated with dupilumab meeting one of the following conditions: -Participants who stopped dupilumab treatment due to non-response, partial response, loss of efficacy must have been previously treated with dupilumab for at least 16 weeks duration; -Participants who stopped dupilumab treatment due to intolerance or adverse events (AEs) to the drug may enter the study with no required prior length of dupilumab treatment; -Participants who stopped dupilumab treatment due to cost or loss of access to dupilumab or for any other reasons may enter the study with no required prior length of dupilumab treatment.
Exclusion: Use of immunosuppressive/immunomodulating drugs and/or therapies, JAK inhibitors, or phototherapy (including tanning booth/parlor) within 4 weeks prior to the Baseline visit; Allergen immunotherapy should be discontinued 6 months before randomization; Have uncontrolled asthma that might require bursts of oral or systemic corticosteriods, or require either of the following due to ≥1 exacerbations within 12 months before Baseline: -Systemic (oral and/or parenteral) corticosteroid treatment; -Hospitalization for >24 hours; Have had systemic treatment with small molecule investigational drugs within 8 weeks or 5 half-lives (if known), whichever is longer, prior to the Baseline visit; Have received treatment with topical corticosteroids (TCS), topical calcineurin inhibitors (TCI) such as tacrolimus and pimecrolimus, topical phosphodiesterase inhibitors such as crisaborole, topical JAK inhibitors (commercial or investigational use), within 1 week prior to randomization; Known diagnosis of active tuberculosis or non-tuberculous mycobacterial infection or latent tuberculosis unless it is well documented by a specialist that the patient has been adequately treated; Have an uncontrolled chronic disease that may require multiple intermittent use of systemic corticosteroids at Screening, as defined by the Investigator; History of human immunodeficiency virus (HIV) or positive HIV serology at Screening; Infected with hepatitis B or hepatitis C viruses. For Hepatitis B, all subjects will undergo testing for Hepatitis B Surface Antigen (HBsAg) and Hepatitis B Core Antibody (HBcAb) during Screening. Subjects who are HBsAg positive are not eligible for the study. Subjects who are HBsAg negative and HBcAb positive will be tested for Hepatitis B Surface Antibody (HBsAb) and if HBsAb is positive, may be enrolled in the study; if HBsAb is negative, the subject is not eligible for the study. For Hepatitis C, all subjects will undergo testing for Hepatitis C antibody (HCVAb) during Screening. Subjects who are HCVAb positive are not eligible for the study. Active COVID-19 infection at Baseline; Have known liver cirrhosis and/or chronic hepatitis of any etiology; Have inadequate organ function or abnormal lab results considered clinically significant by the Investigator at the Screening visit.