Single-Tablet Combination Therapy of Macitentan/Tadalafil for Patients with Pulmonary Arterial Hypertension: Qualitative Interview Study of the A DUE Phase 3 Trial
Jazyk angličtina Země Spojené státy americké Médium print-electronic
Typ dokumentu časopisecké články
PubMed
40100308
PubMed Central
PMC12006254
DOI
10.1007/s12325-025-03159-x
PII: 10.1007/s12325-025-03159-x
Knihovny.cz E-zdroje
- Klíčová slova
- Clinician interview, Fixed-dose combination, Patient interview, Patient perspective, Polypharmacy, Pulmonary arterial hypertension, Treatment adherence,
- MeSH
- adaptivní klinické zkoušky jako téma MeSH
- antihypertenziva * aplikace a dávkování terapeutické užití MeSH
- dospělí MeSH
- dvojitá slepá metoda MeSH
- fixní kombinace léků MeSH
- inhibitory fosfodiesterasy 5 aplikace a dávkování terapeutické užití MeSH
- klinické zkoušky, fáze III jako téma MeSH
- kvalitativní výzkum MeSH
- lidé středního věku MeSH
- lidé MeSH
- multicentrické studie jako téma MeSH
- plicní arteriální hypertenze * farmakoterapie MeSH
- plicní hypertenze * farmakoterapie MeSH
- pyrimidiny * aplikace a dávkování terapeutické užití MeSH
- randomizované kontrolované studie jako téma MeSH
- rozhovory jako téma MeSH
- senioři MeSH
- spokojenost pacientů MeSH
- sulfonamidy * aplikace a dávkování terapeutické užití MeSH
- tablety MeSH
- tadalafil * aplikace a dávkování terapeutické užití MeSH
- Check Tag
- dospělí MeSH
- lidé středního věku MeSH
- lidé MeSH
- mužské pohlaví MeSH
- senioři MeSH
- ženské pohlaví MeSH
- Publikační typ
- časopisecké články MeSH
- Názvy látek
- antihypertenziva * MeSH
- fixní kombinace léků MeSH
- inhibitory fosfodiesterasy 5 MeSH
- macitentan-tadalafil MeSH Prohlížeč
- macitentan MeSH Prohlížeč
- pyrimidiny * MeSH
- sulfonamidy * MeSH
- tablety MeSH
- tadalafil * MeSH
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.
1st Affiliated Hospital of Xi'an Jiaotong University Xi'an Shaanxi China
Charles University and General University Hospital Prague Czech Republic
Clinical Outcomes Solutions Chicago IL USA
Clinical Outcomes Solutions Folkestone UK
Janssen Cilag GmbH a Johnson and Johnson Company Neuss Germany
Janssen Cilag Limited a Johnson and Johnson Company Clinical Science Glasgow UK
Janssen Global Services LLC a Johnson and Johnson Company Horsham PA USA
Janssen Research and Development LLC a Johnson and Johnson Company Titusville NJ USA
Suite 8 Motis Business Centre Cheriton High Street Folkestone Kent T19 4QJ UK
Thoraxklinik at Heidelberg University Hospital Heidelberg Germany
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