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1 the current practice of adding bosentan, an endothelin receptor antagonist.
2 ral phosphodiesterase-5 inhibitor or an oral endothelin-receptor antagonist.
3 terase type 5 inhibitors, sodium nitrite and endothelin receptor antagonists.
4 bitors, niacin, inhaled carbon monoxide, and endothelin receptor antagonists.
5 mineralocorticoid receptor antagonists, and endothelin receptor antagonists.
6 se biological effects that are unaffected by endothelin receptor antagonists.
7 s of disease-targeted therapy (predominantly endothelin receptor antagonists [47.3%] or phosphodieste
8 gated for the treatment of nmCRPC, including endothelin receptor antagonists and bone-targeted therap
9 -3-methyl-glutaryl-CoA reductase inhibitors, endothelin receptor antagonists and phosphodiesterase ty
11 ple, with phosphodiesterase 5 inhibitors and endothelin receptor antagonists) and, if necessary, the
12 he treatment of PAH: prostacyclin analogues, endothelin receptor antagonists, and phosphodiesterase t
16 hese findings raise the possibility of using endothelin receptor antagonists as neuroprotective agent
18 a 12-month trial of bosentan, a nonselective endothelin receptor antagonist, as a therapy for SSc-rel
19 R trial assessed the association between the endothelin receptor antagonist atrasentan and pain and p
22 liminary study, the orally administered dual endothelin-receptor antagonist bosentan improved exercis
24 We investigated whether treatment with the endothelin receptor antagonist, bosentan, decreased the
27 i) may offset fluid retaining effects of the endothelin receptor antagonist (ERA) atrasentan while ef
29 Preclinical studies have demonstrated that endothelin receptor antagonists (ERAs) can reduce or pre
34 s sodium-glucose cotransporter 2 inhibitors, endothelin receptor antagonists, glucagon-like peptide 1
37 rable hemodynamic and neurohormonal effects, endothelin receptor antagonists have not improved outcom
39 mineralocorticoid antagonist and a selective endothelin receptor antagonist, have now been demonstrat
41 In many studies, such as the Study with an Endothelin Receptor Antagonist in Pulmonary Arterial Hyp
42 data support a potential role for selective endothelin receptor antagonists in protecting renal func
43 roenvironment and further support the use of endothelin receptor antagonists in the treatment of inva
44 changes of HPS and the effects of selective endothelin receptor antagonists in vivo were assessed af
45 he efficacy and safety of tezosentan, a dual endothelin receptor antagonist, in patients hospitalized
46 nd safety of tezosentan, an intravenous dual endothelin receptor antagonist, in patients with moderat
47 sess the hemodynamic effects of bosentan, an endothelin receptor antagonist, in patients with PHT, in
52 ar Disease]), we evaluated the effects of an endothelin receptor antagonist, macitentan, in patients
55 Three patients required PH treatment with endothelin receptor antagonist (n=2) or calcium channel
56 us epoprostenol were weaned off post-LT, and endothelin receptor antagonist or phosphodiesterase type
57 y hypoxia but attenuated by either selective endothelin receptor antagonists or oligonucleotides targ
58 were receiving riociguat in combination with endothelin receptor antagonists or prostanoids, or both.
59 hypertension and patients who were receiving endothelin-receptor antagonists or (nonintravenous) pros
61 ials continue to explore new applications of endothelin receptor antagonists, particularly in treatme
63 144-363 d) after the initial combination of endothelin receptor antagonist + phosphodiesterase-5 inh
64 erent classes of drugs are now available-ie, endothelin receptor antagonists, phosphodiesterase-5 inh
68 udy examined the effects of the nonselective endothelin receptor antagonist SB-209,670, and the less
69 For instance, macitentan and bosentan from endothelin receptor antagonists show major concern while
72 Tezosentan is an intravenous short-acting endothelin receptor antagonist that has favorable hemody
74 the efficacy and safety of bosentan, a dual endothelin-receptor antagonist that can be taken orally,
75 mendation for either prostacyclin agonist or endothelin receptor antagonist therapy and a strong reco
77 essed the efficacy of macitentan, a new dual endothelin-receptor antagonist, using a primary end poin
78 n of the endothelin system with bosentan, an endothelin receptor antagonist, was strongly protective
79 pulmonary arterial hypertension, other than endothelin-receptor antagonists, was allowed at study en
81 ts, which have been previously attributed to endothelin receptor antagonists, were more frequent in t
82 as aldosterone synthase inhibitors and dual endothelin receptor antagonists, whereas others may prov
83 g at the identification of novel potent dual endothelin receptor antagonists with high oral efficacy.