A Phase 2 Study of IkT-001Pro in Pulmonary Arterial Hypertension (PAH)

Inclusion Criteria: 1. Men and women between the ages of 18 and 70 years of age (inclusive) at the time of signing the informed consent. 2. Capable of giving signed ICF. 3. Documented diagnostic right heart catheterization (RHC) at any time prior to screening confirming the diagnosis of WHO PAH Group 1 in any of the following subtypes: 1. Idiopathic PAH 2. Heritable PAH 3. Drug/toxin-induced PAH 4. PAH associated with CTD 5. PAH associated with simple, congenital systemic-to-pulmonary shunts at least 1 year following repair 4. Symptomatic PH classified as WHO FC II or III 5. Baseline RHC performed during the Screening Period documenting a minimum PVR of ≥ 400 dyn.sec.cm-5 (≥5 WU) and a pulmonary capillary wedge pressure (PCWP) or left ventricular end-diastolic pressure of ≤ 15 mmHg. a. NOTE: At least 50% of study population needs to have PVR ≥ 800 dyn.sec.cm-5. 6. On stable doses of background PAH therapy (i.e., patient-specific dose goal for each therapy already achieved) for at least 90 days prior to screening; for infusion prostacyclins, dose adjustment within 10% of optimal dose is allowed per medical practice. a. For those taking sotatercept their dosing regimen should be stable for at least 6 months prior to screening 7. 6MWD ≥ 150 and ≤ 500 m repeated twice at screening (measured at least 4 hours apart, but no longer than 1 week), and both values are within 15% of each other (calculated from the highest value). Exclusion Criteria: 1. Diagnosis of PAH WHO Groups 2, 3, 4, or 5 2. Diagnosis of the following PAH Group 1 subtypes: human immunodeficiency virus (HIV)-associated PAH and PAH associated with portal hypertension. Exclusions in PAH Group 1 should also include schistosomiasis-associated PAH and pulmonary veno-occlusive disease 3. Uncontrolled systemic hypertension as evidenced by sitting systolic BP \> 160 mmHg or sitting diastolic BP \> 100 mmHg during screening visit after a period of rest 4. Personal or family history of long QT syndrome (LQTS) or sudden cardiac death 5. Pulmonary function tests (PFT) completed no more than 24 weeks before the screening period (or completed at the Screening Visit). Following criteria must are considered exclusionary 6. Cerebrovascular accident within 3 months prior to the screening visit 7. Currently receiving moderate or strong Cytochrome P450 (CYP) 3A4/5 inducers or CYP3A4/5 inhibitors (except for topical administration) 8. Currently receiving or anticipated need to receive anticoagulants 9. Currently receiving or anticipated need to receive more than one anti-platelet medication. The use of prostacyclins is not considered exclusionary. Note that sotatercept is not considered anti-platelet therapy 10. Initiation of an exercise program for cardiopulmonary rehabilitation within 90 days prior to the screening visit or planned initiation during the study (participants who are stable in the maintenance phase of a program and who will continue for the duration of the study are eligible) 11. History of atrial septostomy within 180 days prior to the screening visit 12. Current participation in another investigational clinical trial and/or receipt of any investigational medication within 90 days prior to screening 13. Estimated glomerular filtration rate (eGFR) \< 30 mL/min/m2 (as defined by the Modification of Diet in Renal Disease \[MDRD\] equation)