A clinical trial looking at the use and safety of tadalafil for the treatment of pulmonary arterial hypertension in children

Mise à jour : Il y a 4 ans
Référence : EUCTR2012-002354-23

Femme et Homme

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Extrait

Period 1 primary objectives: For the EU regulatory assessment, the primary objective of Period 1 is to evaluate the efficacy of tadalafil compared with placebo, as measured by time to clinical worsening (CW) in pediatric PAH patients through Week 24. For the United States (US) regulatory assessment, the primary objective of Period 1 is to evaluate the efficacy of tadalafil compared with placebo in improving 6-minute walk distance from bBaseline to Week-24 as assessed in a subset of patients ≥6 to <18 years of age who are developmentally capable of performing a 6MW test. Period 2 Primary Objective: The primary objective of Period 2 is to evaluate long-term safety of tadalafil while providing continued access to tadalafil for pediatric patients with PAH who participated in Period 1


Critère d'inclusion

  • pulmonary arterial hypertension