Examples of using Macitentan in English and their translations into Greek
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Colloquial
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Official
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Medicine
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Ecclesiastic
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Financial
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Official/political
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Computer
In dogs, macitentan decreased blood pressure at exposures similar to the therapeutic human exposure.
Macitentan is currently investigated in a pivotal Phase III program in patients with ischemic digital ulcers associated with systemic sclerosis, initiated in December 2011.
I truly believe that these results with macitentan will translate into clinical benefits for patients suffering from PAH.
dogs after treatment with macitentan.
Cases of anaemia requiring blood cell transfusion have been reported with macitentan and other ERAs.
a Phase I/Ib open-label study was initiated with macitentan in patients with recurring glioblastoma.
was not affected by macitentan.
The development of testicular tubular atrophy in male animals was observed after treatment with macitentan(see section 5.3).
a strong CYP3A4 inhibitor, exposure to macitentan increased approximately 2-fold.
The safety of macitentan has been evaluated in a long-term placebo-controlled trial of 742 patients with symptomatic PAH.
Due to the high degree of protein binding of macitentan, dialysis is unlikely to be effective.
The safety and efficacy of macitentan in children and adolescents below 18 years have not yet been established.
The mean treatment duration was 103.9 weeks in the macitentan 10 mg group, and 85.3 weeks in the placebo group.
Macitentan may lead to more reduction of blood pressure
Macitentan was not phototoxic in vivo after single dose at exposures of up to 24-fold the human exposure.
There is limited clinical experience with macitentan in patients over the age of 75 years,
In rats, macitentan and its metabolites are excreted into milk during lactation(see section 5.3).
which is approximately 5-fold less potent than macitentan, was approximately 1.3-fold higher than in healthy subjects.
Adverse reactions associated with macitentan obtained from this clinical study are tabulated below.
Macitentan and its active metabolite do not have clinically relevant inhibitory or inducing effects on cytochrome P450 enzymes.