Overview
Phase 1b/2 Study of HS235 Assessing the Safety, Pharmacokinetics, Pharmacodynamics, and Efficacy of the Activin Signaling Inhibitor HS235 Added to Background Treatment in Adults with Pulmonary Arterial Hypertension (PAH)
Description
A Phase 1b/2, Multicenter, Randomized, Double-Blind, Placebo-Controlled, Dose-Ranging Study Assessing the Safety, Pharmacokinetics, Pharmacodynamics, and Efficacy of the Activin Signaling Inhibitor HS235 Added to Background Treatment in Adults with Pulmonary Arterial Hypertension (PAH)
Eligibility
Inclusion Criteria:
Participants are eligible to be included in the study only if they meet all of the following criteria:
- Male and female participants, 18 years of age and older.
- Body Mass Index (BMI) 18.5 and 40 kg/m2 and body weight at or below 120 kg.
- Baseline RHC performed during the Screening Period documenting:
- A minimum PVR of ≥ 5 Wood units (WU) or ≥ 400 dyn·sec·cm-5 and,
- A pulmonary artery wedge pressure (PAWP) of ≤ 15 mm Hg.
- Diagnosis of WHO pulmonary arterial hypertension (PAH) Group 1.
- Symptomatic PAH classified as WHO Functional class II to IV.
- On stable doses of at least 2 approved background PAH therapies and diuretics.
- 6-Minute Walk Distance (6MWD) ≥ 150 m and ≤ 500 m repeated twice during screening.
- Ability to adhere to study visit schedule and understand and comply with all protocol requirements.
Exclusion Criteria:
- PH WHO Groups 2, 3, 4 or 5.
- Hospitalization for any worsening medical condition or major surgery within 4 weeks prior to screening.
- Any symptomatic coronary disease events.
- History of heart transplant or on heart transplant list.
- Uncontrolled systemic hypertension.
- History of restrictive, constrictive or congestive cardiomyopathy.
- History of significant mitral regurgitation or aortic regurgitation valvular disease.
- Untreated or poorly controlled moderate or severe obstructive sleep apnea.
- A diagnosis of worse than moderate COPD or worse than mild ILD.
- Cerebrovascular event within 90 days prior to screening
- A pneumonectomy or lobectomy
- Having received an activin signaling inhibitor such as sotatercept at any time prior to screening
- A Hgb \> sex-specific ULN
- Platelets count \< 100,000/mm3
- Severe (stage ≥4) renal failure with eGFR \< 30 mL/min/m2
- Abnormally elevated liver function enzymes (ALT or AST \> 3X ULN, or total bilirubin \> 1.5X ULN).


