Evidence map›Paper›PMID 38443648›Full record

ArticleAdvances in therapy2024

Study Design of a Phase 2/3 Randomized Controlled Trial of Dupilumab in Adults with Bullous Pemphigoid: LIBERTY-BP ADEPT.

Dédée F Murrell, Pascal Joly, Victoria P Werth, Hideyuki Ujiie, Margitta Worm, Aaron R Mangold, Elena Avetisova, Jennifer Maloney, Elizabeth Laws, Eric Mortensen and 2 more

Erratum issued Registry-linked trialOpen access · hybridAbstract readClinical Trial Protocol
In one paragraph

Article in Advances in therapy, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. It is linked to trial NCT04206553 (A Multicenter, Randomized, Double-Blind, Placebo-Controlled, Parallel Group Study to Evaluate the Efficacy and Safety of Dupilumab in Adult Patients With Bullous Pemphigoid), which is not on this map. Cited by 35 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
35citing papers in PubMed, 3 pooled it
12.3field-weighted citation impact, top 1% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

NCT04206553 phase2 / phase3completednot on this map

A Multicenter, Randomized, Double-Blind, Placebo-Controlled, Parallel Group Study to Evaluate the Efficacy and Safety of Dupilumab in Adult Patients With Bullous Pemphigoid

TypeinterventionalSponsorRegeneron PharmaceuticalsRan2020 to 2025Enrolled106ConditionsBullous PemphigoidArmsdupilumab, Matching Placebo, Oral corticosteroids (OCS)
3 · Its place in the literature

Who cites it

35 citing papers in PubMed, 3 syntheses or guidelines pooled it, 29 citations in OpenAlex.

  1. European S2k guidelines on management of autoimmune blistering diseases in children and adolescents.Journal of the European Academy of Dermatology and Venereology : JEADV · 2026
    Guideline
  2. Pooled it
  3. Pooled it
  4. Emerging Paediatric Uses of Dupilumab Beyond Approvals.Clinical and experimental allergy : journal of the British Society for Allergy and Clinical Immunology · 2026
    Review
  5. [New treatment options for autoimmune bullous diseases].Dermatologie (Heidelberg, Germany) · 2026
    Review
  6. Review
  7. Review
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  12. Review
  13. Dermatology 2.0: Precision medicine for inflammatory skin diseases.Journal of the European Academy of Dermatology and Venereology : JEADV · 2026
    Review
  14. Review
  15. Article
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

12 authors at 9 institutions in 5 countries.

Dédée F MurrellDepartment of Dermatology, St George Hospital, University of New South Wales, Sydney, NSW, Australia. d.murrell@unsw.edu.au.
Pascal JolyRouen University Hospital and INSERM 1234, Normandy University, Rouen, France.
Victoria P WerthPerelman School of Medicine at the University of Pennsylvania, Philadelphia, PA, USA.
Hideyuki UjiieDepartment of Dermatology, Faculty of Medicine and Graduate School of Medicine, Hokkaido University, Sapporo, Japan.
Margitta WormCharité-Universitätsmedizin Berlin, Berlin, Germany.
Aaron R MangoldDepartment of Dermatology, Mayo Clinic, Scottsdale, AZ, USA.
Elena AvetisovaRegeneron Pharmaceuticals Inc., Tarrytown, NY, USA.
Jennifer MaloneyRegeneron Pharmaceuticals Inc., Tarrytown, NY, USA.
Elizabeth LawsSanofi, Bridgewater, NJ, USA.
Eric MortensenRegeneron Pharmaceuticals Inc., Tarrytown, NY, USA.
Ariane Dubost-BramaSanofi, Chilly-Mazarin, France.
Arsalan ShabbirRegeneron Pharmaceuticals Inc., Tarrytown, NY, USA.
Regeneron (United States) · USCharité - Universitätsmedizin Berlin · DEHokkaido University · JPMayo Clinic in Arizona · USSanofi (France) · FRSanofi (United States) · USSt George Hospital · AUUniversité de Rouen Normandie · FRUniversity of Pennsylvania · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundBullous pemphigoid (BP) is a rare, autoimmune, blistering skin disease associated with high disease burden, profoundly decreased quality of life and increased morbidity. Emerging evidence supports an important role for type 2 inflammation in disease pathogenesis. Current management relies on topical and/or systemic corticosteroids, non-selective immunosuppressants and antibiotics with anti-inflammatory properties, which are all limited by side effects and toxicities. Therefore, targeted, efficacious and safe therapies are needed. Dupilumab blocks the shared receptor component for interleukin (IL)-4 and IL-13, key and central drivers of type 2 inflammation. Several reports of patients successfully treated with dupilumab have been published; however, dupilumab has not been formally assessed in a double-blind, placebo-controlled trial.

objectivesWe report the design of LIBERTY-BP ADEPT, a multicenter, randomized, double-blind, placebo-controlled clinical trial to evaluate the efficacy and safety of dupilumab in adults with BP.

methodsLIBERTY-BP ADEPT comprises a 35-day screening, 52-week treatment and 12-week follow-up period. Approximately 98 adults aged 18-90 years with moderate-to-severe BP are being enrolled at 51 sites on 4 continents and randomized 1:1 to subcutaneous dupilumab or placebo every 2 weeks. All participants will receive concomitant oral corticosteroids (OCS). PLANNED OUTCOMES: The primary endpoint is the proportion of patients achieving complete remission off steroid therapy at week 36. Key secondary endpoints include total cumulative OCS dose to week 36, percent change and proportion of patients with ≥ 4-point reduction in the weekly average of daily Peak Pruritus Numerical Rating Scale from baseline to week 36 and percent change in Bullous Pemphigoid Area Index score from baseline to week 36.

conclusionThe trial results will provide evidence on whether the efficacy and safety of dupilumab support its use as a potential novel treatment approach for BP and will provide new insights into the role of type 2 inflammation in BP pathogenesis. CLINICAL

trial registrationClinicalTrials.gov identifier NCT04206553.

Indexed as

Antibodies, Monoclonal, HumanizedPemphigoid, BullousAdultAgedClinical Trials, Phase II as TopicClinical Trials, Phase III as TopicDouble-Blind MethodFemaleHumansMaleMiddle AgedRandomized Controlled Trials as TopicTreatment OutcomeAntibodies, Monoclonal, HumanizeddupilumabAutoimmune blistering disorderBullous pemphigoidDupilumabOral corticosteroids

Identifiers

PMID38443648
PMCPMC11213798
OpenAlexW4392448313

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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Registered trials

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.