DeCastro Carlos, Sheinberg Phillip, Han Bing, Vallow Susan, Bermann Georgina, Dhalke Marion, Kumar Rakesh, Dickie Gavin, Galipeau Nina, Lamoureux Roger, Rupinski Kaelyn, Lowe Caitlyn, Nieves Amber, de Fontbrune Flore Sicre, de Latour Regis Peffault
Duke University Medical Center, Durham, NC, USA.
Hospital A Beneficência Portuguesa, Sao Paolo, Brazil.
Patient. 2025 Jul 22. doi: 10.1007/s40271-025-00755-5.
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.
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.
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.
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.
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).
阵发性睡眠性血红蛋白尿(PNH)是一种罕见的血液疾病,症状包括疲劳、呼吸困难和血红蛋白尿,这些症状会对健康相关生活质量产生负面影响。
对参与三项临床试验的PNH患者进行试验期间访谈,以了解患者在接受新型PNH治疗药物依他库帕后(iptacopan)的体验和满意度。
招募成年PNH参与者并同意其参与三项依他库帕II/III期试验(NCT04558918、NCT04820530和NCT04747613)中的定性访谈。访谈文件由目标国家的相关伦理机构制定并批准。经过培训的定性访谈人员使用半结构化访谈指南,以获取有关PNH相关症状的信息,以及参与者在试验前经历的影响、接受依他库帕后这些情况如何变化,以及他们的治疗体验和对依他库帕的满意度。
在八个国家对61名参与者进行了访谈。参与者报告了与PNH相关的广泛症状和影响,包括疲劳、疲倦、沮丧、难以进行日常活动以及社交活动受限。访谈参与者报告称,接受依他库帕后,PNH的体征、症状和影响有所改善,大多数参与者认为这些改善意义重大。参与者报告对依他库帕的治疗体验“非常满意”或“满意”。
这些访谈的结果提供了有价值的患者报告数据,表明接受依他库帕后患者有积极的治疗体验,PNH症状及与健康相关的生活质量影响有显著改善。患者的这些定性报告支持了依他库帕三项临床试验中显示的积极疗效结果,并提供了背景信息。NCT04558918(2020年9月16日),NCT04820530(2021年3月25日),NCT04747613(2021年2月9日)。