
Sotatercept, a first-in-class activin signalling inhibitor for pulmonary arterial hypertension (PAH), is approved in Hong Kong in August 2025,following regulatory approvals in Macau, the US, and the EU in February 2025.
The fourth pathway: A potential game-changer?
PAH is a rare, severe progressive disorder characterized by proliferative remodelling of small pulmonary arteries and progressive luminal narrowing. This stems from an imbalance in the antiproliferative (BMPR-II– mediated) and proproliferative (activin receptor type IIA [ActRIIA]– mediated) signalling pathways. [Cardiol Clin 2016;34:363-374; N Engl J Med 2023;388:1478-1490; Eur Respir J 2023;61:2201347]
Over the past 20 years, PAH therapies have primarily focused on promoting vasodilation through targeting the endothelin-1 (ET-1), nitric oxide (NO), and prostacyclin (PGI2) pathways. Although the treatment approach has shifted from targeting an individual pathway to more aggressive, earlier use of combination therapy, morbidity and mortality have remained high, underscoring the need for new treatment options that target pathways involved in pulmonary vascular remodelling. [N Engl J Med 2023;388:1478- 1490; Int J Cardiol Congenital Heart Disease 2025;doi:10.1016/j.ijcchd.2025.100594]
Sotatercept, a first-in-class activin signalling inhibitor, aims to restore the balance between the antiproliferative and proproliferative signalling pathways. Unlike current vasodilatory therapies, sotatercept holds promise as a disease-modifying therapy because it targets the underlying pathophysiological mechanism in PAH. [Int J Cardiol Congenital Heart Disease 2025;doi:10.1016/j.ijcchd.2025.100594; Expert Opin Ther Targets 2025;29:327-343]
Improved exercise capacity
STELLAR, a multicentre, double-blind, phase III trial, evaluated the efficacy and safety of sotatercept in 323 adult patients (median age, 47.9 years; female, 79.3 percent) with PAH (WHO Group 1, functional class II [48.6 percent] or III [51.4 percent]) who were receiving stable background therapy (triple therapy, 61.3 percent; prostacyclin infusion therapy, 39.9 percent; double therapy, 34.7 percent; monotherapy, 4.0 percent). Patients were randomized 1:1 to receive subcutaneous sotatercept (starting dose, 0.3 mg/kg of body weight; target dose, 0.7 mg/ kg) or placebo Q3W. [N Engl J Med 2023;388:1478-1490]
STELLAR met its primary endpoint by demonstrating a significant improvement from baseline in 6-minute walk distance (6MWD) at week 24 with sotatercept vs placebo (40.8 meters; 95 percent confidence interval [CI], 27.5–54.1; p<0.001), indicating improved exercise capacity.
Reduced risk of death or clinical worsening
Notably, treatment with sotatercept resulted in an 84 percent lower risk of a composite of death from any cause or nonfatal clinical worsening event (a secondary endpoint) (5.5 vs 26.2 percent; hazard ratio [HR], 0.16; 95 percent CI, 0.08–0.35; p<0.001) vs placebo.
At week 24, statistically significant improvements with sotatercept were also reported in the majority of other prespecified secondary endpoints, including:
- Multicomponent improvement (defined as meeting all three criteria: 6MWD, N-terminal pro-B-type natriuretic peptide [NT-proBNP] level, and WHO functional class; 38.9 vs 10.1 percent; p<0.001);
- Pulmonary vascular resistance (PVR; difference, -234.6 dyn·sec/ cm5; p<0.001);
- NT-proBNP level (difference, -441.6 pg/mL; p<0.001);
- WHO functional class improvement (29.4 vs 13.8 percent; p<0.001);
- French low-risk risk score (39.5 vs 18.2 percent; p<0.001);
- PAH–Symptoms and Impact (PAH-SYMPACT) Physical Impacts domain score (difference, -0.26; p<0.05);
- PAH-SYMPACT Cardiopulmonary Symptoms domain score (difference, -0.13; p<0.05).
However, the PAH-SYMPACT Cognitive/Emotional Impacts domain score, which was assessed as the final secondary outcome measure, did not show a statistically significant difference between the sotatercept and placebo groups (p>0.05).
Improved haemodynamics and right heart function
A post-hoc analysis of STELLAR demonstrated improvements in right heart catheterization (RHC) and echocardiographic parameters with sotatercept vs placebo, which may reflect partial remodelling of pulmonary arteries. [Eur Respir J 2023;62:2301107]
Sotatercept significantly reduced mean pulmonary artery pressure (mPAP) — a hallmark feature of PAH — by 13.9 mm Hg (p<0.0001), indicating a decrease in pressure within the pulmonary circulation.
Furthermore, sotatercept significantly improved PVR (-254.8 dyn·s/ cm5; p<0.0001), mean right atrial pressure (-2.7 mm Hg; p<0.0001), mixed venous oxygen saturation (3.84 percent; p<0.0001), pulmonary artery elastance (-0.42 mm Hg/mL·beat; p<0.0001), pulmonary artery compliance (0.58 mL/mm Hg ;p<0.0001), cardiac efficiency (0.48 mL/beat·mm Hg; p<0.0001), right ventricular (RV) work (-0.85 g·m; p<0.0001), and RV power (-32.70 mm Hg·L/min; p<0.0001), indicating reduction in workload and energy expenditure of the RV with enhanced cardiac efficiency.
Echocardiography showed improvements in tricuspid annular plane systolic excursion to systolic pulmonary artery pressure (TAPSE/sPAP) ratio (0.12 mm/mm Hg; p<0.0001), end-systolic and end-diastolic RV areas (-4.39 cm2 and -5.31 cm2, respectively; both p<0.0001), as well as tricuspid regurgitation and RV fractional area change (2.04 percent; p<0.05).
Collectively, these findings suggest that sotatercept treatment exerts beneficial effects on right heart function and dimensions by reducing PA pressure and RV workload in patients with PAH.
Lower incidence of AEs vs placebo
The safety profile of sotatercept in the STELLAR trial was consistent with that observed in the phase II PULSAR trial and its extension study. [N Engl J Med 2023;388:1478-1490; N Engl J Med 2021;384:1204-1215; Eur Respir J 2023;61:2201347]
Rates of overall adverse events (AEs; 84.7 vs 87.5 percent), severe AEs (8.0 vs 13.1 percent), and serious AEs (14.1 vs 22.5 percent) at week 24 were numerically lower with sotatercept than placebo. Fewer patients in the sotatercept vs placebo group discontinued the trial regimen owing to AEs (1.8 vs 6.2 percent). [N Engl J Med 2023;388:1478-1490]
AEs that occurred more frequently with sotatercept than placebo included epistaxis (12.3 vs 1.9 percent), dizziness (10.4 vs 1.9 percent), telangiectasia (10.4 vs 3.1 percent), thrombocytopenia (6.1 vs 2.5 percent), increased haemoglobin levels (5.5 vs 0 percent), and increased blood pressure (3.7 vs 0.6 percent).
Early termination of two trials in view of overwhelming efficacy data
The recently published phase III ZENITH trial of sotatercept demonstrated a 76 percent reduction in risk of death, lung transplantation, or PAH-related hospitalization vs placebo in patients with PAH at high risk of death. The trial was stopped early due to overwhelming efficacy data. [N Engl J Med 2025;392:1987-2200]
The phase III HYPERION trial in PAH patients with newly diagnosed intermediate- or high-risk PAH was also stopped prematurely due to positive results from ZENITH along with the totality of data from sotatercept’s clinical trial programme. In other words, the HYPERION trial has lost its clinical equipoise and it became no longer ethical to withhold the beneficial treatment from the control group. As a result, all study participants are now able to access sotatercept treatment. [NCT04811092; www.merck. com/news/merck-announces-decision-to-stop-phase-3-hyperion-trial-evaluating-winrevair-sotatercept-csrk-early-and-move-to-final-analysis]