Single-Tablet Combination Therapy of Macitentan/Tadalafil for Patients with Pulmonary Arterial Hypertension: Qualitative Interview Study of the A DUE Phase 3 Trial

IF 3.4 3区 医学 Q2 MEDICINE, RESEARCH & EXPERIMENTAL
Fenling Fan, Stacy Davis, Claire Burbridge, Kelly Chin, Michael Friberg, Ekkehard Grünig, Melanie Hughes, Pavel Jansa, Jörg Linder, Jennifer Rafalski, Alvaro Agustin Rodriguez, Jason A. Randall
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Abstract

Introduction

This study explored patient and clinician perspectives on a new fixed-dose combination of macitentan and tadalafil (M/T FDC) in a once-daily single tablet for treatment of pulmonary arterial hypertension (PAH).

Methods

Qualitative semi-structured interviews were conducted during the open-label period of the global, phase 3 A DUE clinical trial that evaluated M/T FDC. A subset of enrolled patients (N = 26) and site investigators (N = 18 clinicians) were interviewed. Patients received four tablets during double-blind treatment and could be in one of three arms (macitentan + placebo; tadalafil + placebo; M/T FDC + placebo) followed by M/T FDC (one tablet) during the open-label period. Patients and clinicians were asked to share their experience of pre-trial PAH medication, double-blind treatment, and open-label M/T FDC. Thematic analysis was conducted on blinded data.

Results

Patients preferred the M/T FDC tablet (open-label) over the four tablets during double-blind treatment. Patients were satisfied with M/T FDC, highlighting its positive impact on their psychological well-being, through reducing stress associated with managing multiple pills. All patients indicated that having a single, once-a-day pill for PAH was more convenient and associated with greater treatment adherence. Clinicians highlighted that their patients have a high daily pill burden for PAH and other comorbidities, and prefer treatments with an oral mode of administration that reduce the number of daily pills required. Clinicians felt that M/T FDC would be well received in clinical practice and potentially assist in implementing guideline-recommended combination treatment of PAH.

Conclusions

In this qualitative analysis, all 26 patients and 18 clinicians provided positive feedback on M/T FDC treatment, which was consistent across countries. Reducing the number of pills needed to treat PAH, through use of single-tablet M/T FDC, is highly valued by patients and endorsed by clinicians, who both felt the single-tablet combination therapy could have a positive effect on patients’ well-being and increase treatment adherence.

马西坦/他达拉非单片联合治疗肺动脉高压:A DUE 3期临床试验的定性访谈研究
简介:本研究探讨了患者和临床医生对每日一次单片马西坦和他达拉非(M/T FDC)新固定剂量组合治疗肺动脉高压(PAH)的看法。方法:在评估M/T FDC的全球3期DUE临床试验的开放标签期间进行定性半结构化访谈。对入选患者(N = 26)和现场调查人员(N = 18名临床医生)进行了访谈。患者在双盲治疗期间接受4片,可分为3组(马西坦+安慰剂;他达拉非+安慰剂;在开放标签期间,M/T FDC +安慰剂),然后是M/T FDC(一片)。患者和临床医生被要求分享他们在试验前多环芳烃药物治疗、双盲治疗和开放标签M/T FDC方面的经验。对盲法数据进行专题分析。结果:在双盲治疗中,患者更倾向于M/T FDC片(开放标签)。患者对M/T FDC感到满意,强调其对心理健康的积极影响,通过减少与服用多种药物相关的压力。所有患者都表示,每天服用一次单药治疗多环芳烃更方便,并与更强的治疗依从性相关。临床医生强调,他们的患者对多环芳烃和其他合并症有很高的每日服药负担,他们更倾向于口服给药,以减少每日服药的数量。临床医生认为M/T FDC在临床实践中会很受欢迎,并可能有助于实施指南推荐的多环芳烃联合治疗。结论:在这一定性分析中,所有26名患者和18名临床医生都对药物/T FDC治疗提供了积极反馈,这在各国是一致的。通过使用单片M/T FDC来减少治疗PAH所需的药片数量,受到患者的高度重视,并得到临床医生的认可,他们都认为单片联合治疗可以对患者的健康产生积极影响,并增加治疗依从性。
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来源期刊
Advances in Therapy
Advances in Therapy 医学-药学
CiteScore
7.20
自引率
2.60%
发文量
353
审稿时长
6-12 weeks
期刊介绍: Advances in Therapy is an international, peer reviewed, rapid-publication (peer review in 2 weeks, published 3–4 weeks from acceptance) journal dedicated to the publication of high-quality clinical (all phases), observational, real-world, and health outcomes research around the discovery, development, and use of therapeutics and interventions (including devices) across all therapeutic areas. Studies relating to diagnostics and diagnosis, pharmacoeconomics, public health, epidemiology, quality of life, and patient care, management, and education are also encouraged. The journal is of interest to a broad audience of healthcare professionals and publishes original research, reviews, communications and letters. The journal is read by a global audience and receives submissions from all over the world. Advances in Therapy will consider all scientifically sound research be it positive, confirmatory or negative data. Submissions are welcomed whether they relate to an international and/or a country-specific audience, something that is crucially important when researchers are trying to target more specific patient populations. This inclusive approach allows the journal to assist in the dissemination of all scientifically and ethically sound research.
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