The search for effective treatments for pulmonary hypertension (PH) has been frustrating. The very first drug for idiopathic pulmonary arterial hypertension (PAH), epoprostenol, was approved in 1995.[1] And while progress has been made, a look at where we were, where we are, and where we need to be suggests we are far from accomplishing our goals.[2] We have identified three classes of drugs th...