PHIRST-1: Tadalafil in the Treatment of Pulmonary Arterial Hypertension

Inclusion Criteria: At least 12 years of age. Body weight at least 40 kg (approximately 88 pounds). Pulmonary hypertension (PAH) that is either idiopathic; related to collagen vascular disease; related to anorexigen use; associated with an atrial septal defect (resting SaO2 greater than or equal to 88%); with surgical repair, of at least 1 year duration, of a congenital systemic-to-pulmonary shunt. If on bosentan, must be at the maximal dose of 125 mg twice daily for a minimum of 12 weeks prior to screening and have an AST/ALT less than 3 times normal. History of PAH established by a resting mean pulmonary artery pressure greater than or equal to 25 mm Hg, pulmonary artery wedge pressure less than or equal to 15 mm Hg, and pulmonary vascular resistance greater than or equal to 3 Wood units via right heart catheterization Have World Health Organization functional class I, II, III or IV status. Have a qualifying 6-minute walk test distance at screening Have no evidence of significant parenchymal lung disease Exclusion Criteria: Are nursing or pregnant. PAH due to conditions other than noted in the above inclusion criteria. History of left-sided heart disease. History of atrial septostomy within 3 months before study entry History of angina pectoris or other condition that was treated with long-or short-acting nitrates within 12 weeks before administration of study drug. History of symptomatic coronary disease. Have any therapy with a prostacyclin or analogue, L-arginine, phosphodiesterase (PDE) inhibitor, or investigational drug within 4 weeks before administration of study drug.