For children on triple therapy with a prostanoid, 27% were in WHO FC III/IV at baseline assessment compared to no children at post‐switch completion assessment at 12.2 [12.0, 13.5] weeks, although this did not reach statistical significance.
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Safety, tolerability, and efficacy of an in-class combination therapy switch from bosentan plus sildenafil to ambrisentan plus tadalafil in children with pulmonary arterial hypertension.
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