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Patient-Reported Meaningful Change in Symptoms and Impacts of Paroxysmal Nocturnal Hemoglobinuria (PNH) in Three Phase III Clinical Trials of Iptacopan

Author

Listed:
  • Carlos DeCastro

    (Duke University Medical Center)

  • Phillip Sheinberg

    (Hospital A Beneficência Portuguesa)

  • Bing Han

    (Chinese Academe of Medical Science)

  • Susan Vallow

    (Novartis AG)

  • Georgina Bermann

    (Novartis AG)

  • Marion Dhalke

    (Novartis AG)

  • Rakesh Kumar

    (Novartis AG)

  • Gavin Dickie

    (Adelphi Values LLC)

  • Nina Galipeau

    (Adelphi Values LLC)

  • Roger Lamoureux

    (Adelphi Values LLC)

  • Kaelyn Rupinski

    (Adelphi Values LLC)

  • Caitlyn Lowe

    (Adelphi Values LLC)

  • Amber Nieves

    (Adelphi Values LLC)

  • Flore Sicre Fontbrune

    (APHP)

  • Regis Peffault Latour

    (Hôpital Saint-Louis)

Abstract

Background Paroxysmal nocturnal hemoglobinuria (PNH) is a rare hematological disease, with symptoms including fatigue, difficulty breathing, and hemoglobinuria, which negatively affect health-related quality of life. Objective In-trial interviews with patients with PNH, enrolled across three clinical trials, were conducted to understand patient experiences and satisfaction after receiving iptacopan, a novel treatment for PNH. Methods Adult participants with PNH were recruited and consented into the qualitative interviews across three phase II/III iptacopan trials (NCT04558918, NCT04820530, and NCT04747613). Interview documents were developed and approved by the relevant ethics authorities in target countries. Trained qualitative interviewers used a semi-structured interview guide to elicit information on PNH-related symptoms and impacts participants experienced prior to the trial, how these changed after receiving iptacopan, and their treatment experience and satisfaction with iptacopan. Results Interviews were conducted with 61 participants in eight countries. Participants reported a broad range of symptoms and impacts associated with PNH, including fatigue, tiredness, frustration, difficulty doing usual activities, and limitation to social activities. Interview participants reported improvements in the signs, symptoms, and impacts of PNH after receiving iptacopan, and the majority of participants considered those improvements to be meaningful. Participants reported being either “very satisfied” or “satisfied” with their treatment experience of iptacopan. Conclusion Findings from these interviews provide valuable patient-reported data on the positive treatment experience and meaningful improvements in PNH symptoms and health-related quality-of-life impacts patients reported after receiving iptacopan. These qualitative reports from patients support and contextualize the positive efficacy results demonstrated in the three iptacopan clinical trials. NCT04558918 (16 Sep 2020), NCT04820530 (25 Mar 2021), NCT04747613 (09 Feb 2021).

Suggested Citation

  • Carlos DeCastro & Phillip Sheinberg & Bing Han & Susan Vallow & Georgina Bermann & Marion Dhalke & Rakesh Kumar & Gavin Dickie & Nina Galipeau & Roger Lamoureux & Kaelyn Rupinski & Caitlyn Lowe & Ambe, 2025. "Patient-Reported Meaningful Change in Symptoms and Impacts of Paroxysmal Nocturnal Hemoglobinuria (PNH) in Three Phase III Clinical Trials of Iptacopan," The Patient: Patient-Centered Outcomes Research, Springer;International Academy of Health Preference Research, vol. 18(6), pages 699-712, November.
  • Handle: RePEc:spr:patien:v:18:y:2025:i:6:d:10.1007_s40271-025-00755-5
    DOI: 10.1007/s40271-025-00755-5
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