Sotatercept: A first-in-class PAH medication approved in HK

20 Aug 2025
Sotatercept: A first-in-class PAH medication approved in HK

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]