Evidence map›Paper›PMID 39934837›Full record

Trial reportOrphanet journal of rare diseases2025

The patient experience of CHAPLE disease: results from interviews conducted as part of a clinical trial for an ultra-rare condition.

Leighann Litcher-Kelly, Ahmet Ozen, Sarah Ollis, Hagit Baris Feldman, Andrew Yaworsky, Paolo Medrano, Voranush Chongsrisawat, Lorah Perlee, Marisa Walker, Sharanya Pradeep and 6 more

Registry-linked trialAbstract readClinical Trial, Phase IIClinical Trial, Phase IIIMulticenter Study
In one paragraph

Trial report in Orphanet journal of rare diseases, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT04209634 (An Open-Label Efficacy and Safety Study of Pozelimab in Patients With CD55-Deficient Protein-Losing Enteropathy), which is not on this map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
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.

NCT04209634 phase2 / phase3completednot on this map

An Open-Label Efficacy and Safety Study of Pozelimab in Patients With CD55-Deficient Protein-Losing Enteropathy (CHAPLE Disease)

TypeinterventionalSponsorRegeneron PharmaceuticalsRan2020 to 2024Enrolled10ConditionsCD55-deficient Protein-losing Enteropathy, CHAPLEArmsPozelimab
3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

16 authors.

Leighann Litcher-KellyAdelphi Values, Boston, MA, USA.
Ahmet OzenMarmara University, Istanbul, Türkiye.
Sarah OllisAdelphi Values, Boston, MA, USA.
Hagit Baris FeldmanTel Aviv Sourasky Medical Center, Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel.
Andrew YaworskyAdelphi Values, Boston, MA, USA.
Paolo MedranoAdelphi Values, Boston, MA, USA.
Voranush ChongsrisawatDepartment of Pediatrics, Faculty of Medicine, Chulalongkorn University, King Chulalongkorn Memorial Hospital, Thai Red Cross Society, Patumwan, Bangkok, Thailand.
Lorah PerleeRegeneron Pharmaceuticals, Inc., Tarrytown, NY, USA.
Marisa WalkerAdelphi Values, Boston, MA, USA.
Sharanya PradeepAdelphi Values, Boston, MA, USA.
Diane M Turner-BowkerAdelphi Values, Boston, MA, USA.
Alina KurolapThe Genetics Institute and Genomics Center, Tel Aviv Sourasky Medical Center, Tel Aviv, Israel.
Orly Eshach AdivHead of Pediatric Gastroenterology and Nutrition Unit, "Hillel Yaffe" Medical Center, Hadera, Israel.
Michael J LenardoMolecular Development of the Immune System Section, Laboratory of Immune System Biology, Laboratory of Clinical Immunology and Microbiology, and Clinical Genomics Program, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, MD, USA.
Olivier A HarariRegeneron Pharmaceuticals, Inc., Tarrytown, NY, USA.
Jessica J JalbertRegeneron Pharmaceuticals, Inc., Tarrytown, NY, USA. jessica.jalbert@regeneron.com.ORCID http://orcid.org/0000-0001-8566-6466

Funding

Division of Intramural Research, National Institute of Allergy and Infectious Diseases Not applicableRegeneron Pharmaceuticals Not applicable
6 · The paper itself

Abstract

backgroundCD55 deficiency with hyper-activation of complement, angiopathic thrombosis, and protein-losing enteropathy (CHAPLE) disease is a newly identified condition with an estimated worldwide prevalence of < 100 patients. Patient interviews can ensure that what is important to patients is assessed in a clinical trial program. Due to the rare and potentially fatal nature of CHAPLE disease, interviews were conducted as part of the pozelimab clinical trial, rather than in a separate study before the trial. The aim of the interviews was to identify the key disease-related signs, symptoms, and health-related quality-of-life (HRQoL) impacts that are important and relevant to patients with CHAPLE disease.

methodsInterviews were conducted with patients and/or caregivers at two timepoints (screening and Week 24) during the pozelimab trial to document the signs/symptoms and HRQoL impacts of CHAPLE disease, and document the most bothersome sign/symptom at screening. At Week 24, interviews gathered additional information on the patient experience from caregivers and patients (note: the impact of pozelimab treatment was also collected, though these results are presented elsewhere).

resultsTen patients, aged 3-19 years, were enrolled in the trial; caregivers contributed to nine interviews. Thirty-one signs‌/symptoms and 65 HRQoL impacts were reported during the interviews. Abdominal pain, diarrhea, facial and peripheral edema/‌swelling, nausea, and vomiting emerged as the core signs/‌symptoms of CHAPLE disease (i.e., experienced by ≥ 90% of patients prior to treatment). The remaining 25 signs/symptoms were experienced by four or fewer (n ≤ 4, ≤ 40.0%) patients, and 15 were only reported by one patient each. Abdominal pain and facial edema were reported as the most bothersome signs/‌symptoms (n = 9, 90.0% and n = 1, 10.0%, respectively). The most frequently reported (i.e., ≥ 80% of interviews) HRQoL impacts were restricted diet (n = 10, 100.0%), sleep disruptions (n = 10, 100.0%), missing school (n = 9, 90.0%), ability to get dressed independently (n = 8, 80.0%), and difficulty engaging in play activities (n = 8, 80.0%).

conclusionsThe main finding from these patient interviews is the identification of six core signs/symptoms of CHAPLE disease: abdominal pain, diarrhea, facial edema/swelling, peripheral edema/swelling, nausea, and vomiting. The severity of the core signs/symptoms leads to substantial impacts on patients' lives.

trial registrationClinicalTrials.gov, NCT04209634. Registered 20 December 2019 https://classic. CLINICALTRIALS: gov/ct2/show/NCT04209634 .

Indexed as

Protein-Losing EnteropathiesRare DiseasesThrombosisAdolescentAdultChildChild, PreschoolFemaleHumansMaleQuality of LifeYoung AdultCHAPLEHRQoLPozelimabWithin-trial interviews

Identifiers

PMID39934837
PMCPMC11817392

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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.