Acute Dosing of MK-8892 in Participants With Pulmonary Arterial Hypertension (PAH) (MK-8892-003)

Inclusion Criteria: * postmenopausal female or if female of reproductive potential, remains abstinent or uses two acceptable methods of birth control during 14 days after dosing with MK-8892 * has suspected PAH classified in one of the following sub-groups: idiopathic, heritable, drug- or toxin-induced, or associated with connective tissue disease, as defined by the Dana Point 2008 Clinical Classification * has a clinical indication for right heart catheterization * PAH classified as World Health Organization (WHO) functional class II or III Exclusion Criteria: * has a medical history indicating a secondary cause of Pulmonary Hypertension (PH) or a non-included etiology of PAH including the following tests within 6 months of Visit 1: Echo indicating significant left heart disease, valvular disease, or structural defects; function test indicating significant pulmonary disease; imaging test indicating veno-occlusive disease; perfusion scan indicating thromboembolic disease; abdominal ultrasound indicating cirrhosis; positive test for human immunodeficiency virus (HIV) * has persistent or permanent atrial fibrillation, significantly impaired gas exchange, history of radiation of the lung or mediastinum, hepatic or hepatobiliary disease, immunodeficiencies or latent bleeding risk * has estimated Glomerular Filtration Rate (GFR) \<45 mL/min * has alanine aminotransferase test (ALT) serum glutamic pyruvic transaminase (SGPT) or aspartate aminotransferase test (AST) serum glutamic oxaloacetic transaminase (SGOT) \>= 3 x upper limit of normal (ULN) at Visit 1 * has a systolic blood pressure (BP) \<105 mmHg, or heart rate (HR) \> 100 beats/min at Visit 1 (Day -7 to -1) * has previously received specific therapy for PAH within 4 weeks prior to Visit 1 * has taken sildenafil, valdenafil or a nitrate within 24 hours prior to Visit 2 date * has taken tadalafil within 7 days prior to Visit 2 date * has taken 2 or more specific PAH medications concomitantly within 4 weeks of anticipated Visit 2 date. Only treatment naïve subjects or subjects on stable PAH-specific monotherapy with an endothelin receptor antagonist (\[ERA\]; bosentan, ambrisentan, or macitentan) or a prostacyclin analog (\[PCA\]; treprostinil, epoprostenol, or iloprost) are eligible. PAH monotherapy with one of these medications may continue without interruption during this study * has taken a soluble guanylate cyclase (sGC) activator (riociguat) within 24 hours of anticipated Visit 2 date. * has taken diltiazem immediate release within 1 day or diltiazem extended release within 2 days prior to Visit 2 date * is currently taking potent inhibitors or inducers of Cytochrome P450 3A4 (CYPA4), or is consuming \>1 liter of grapefruit juice per day * is pregnant or breastfeeding or expecting to conceive during study or post study follow-up period * has donated 500 mL of blood within prior 60 days * is currently participating in or has within the prior three months participated in a study with an investigational compound or device