FDA Approves New Orphan Drug for Treatment of Pulmonary Arterial Hypertension (PAH). The U.S. Food and Drug Administration today approved Letairis (ambrisentan) for the treatment of PAH. Letairis significantly improved physical activity capacity compared with a placebo, as shown by a six-minute walk, a standard test. Letairis also delayed the worsening of the pulmonary hypertension. FDA News. 06/15/07.