Riociguat treatment for portopulmonary hypertension: a subgroup analysis from the PATENT-1/-2 studies
In patients with portopulmonary hypertension (n = 13) included in the 12-week randomized placebo-controlled PATENT-1 trial, riociguat was well tolerated and improved 6-min walking distance (6MWD), World Health Organization functional class (WHO FC), and other efficacy parameters; 6MWD and WHO FC imp...
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Veröffentlicht in: | Pulmonary circulation 2018-04, Vol.8 (2), p.1-4 |
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Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | In patients with portopulmonary hypertension (n = 13) included in the 12-week randomized placebo-controlled PATENT-1 trial, riociguat was well tolerated and improved 6-min walking distance (6MWD), World Health Organization functional class (WHO FC), and other efficacy parameters; 6MWD and WHO FC improvements were sustained over two years in the open-label extension, PATENT-2. |
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ISSN: | 2045-8940 2045-8932 2045-8940 |
DOI: | 10.1177/2045894018769305 |