A Study of Sotatercept for the Treatment of Pulmonary Arterial Hypertension (STELLAR)

Overview

About this study

The purpose of this study is to evaluate the effectiveness and safety of Sotatercept treatment (plus background PAH therapy) versus placebo (plus background PAH therapy) at 24 weeks in adults with Pulmonary Arterial Hypertension (PAH).

Participation eligibility

Participant eligibility includes age, gender, type and stage of disease, and previous treatments or health concerns. Guidelines differ from study to study, and identify who can or cannot participate. There is no guarantee that every individual who qualifies and wants to participate in a trial will be enrolled. Contact the study team to discuss study eligibility and potential participation.

Inclusion Criteria:

  • Age ≥ 18 years.
  • Documented diagnostic right heart catheterization (RHC) at any time prior to screening confirming the diagnosis of WHO pulmonary arterial hypertension (PAH) Group .1 in any of the following subtypes:
    • Idiopathic PAH;
    • Heritable PAH;
    • Drug/toxin-induced PAH;
    • PAH associated with connective tissue disease;
    • PAH associated with simple, congenital systemic-to-pulmonary shunts at least 1 year following repair.
  • Symptomatic PAH classified as WHO Functional Class II or III.
  • Baseline RHC performed during the Screening Period documenting a minimum PVR of ≥ 5 WU and a pulmonary capillary wedge pressure (PCWP) or left ventricular end-diastolic pressure of ≤ 15 mmHg.
  • On stable doses of background PAH therapy and diuretics (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.  Stable diuretic therapy is defined as no addition of a new diuretic and no switching of a pre-existent oral diuretic to parenteral administration; however, dose adjustments (up or down) in pre-existent oral diuretics are acceptable.
  • 6MWD 2: 150 and :S 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).
  • Females of childbearing potential must:
    • Have 2 negative urine or serum pregnancy tests as verified by the investigator prior to starting study therapy; she must agree to ongoing urine or serum pregnancy testing during the study and until 8 weeks after the last dose of the study drug;
    • If sexually active, have used, and agree to use, highly effective contraception without interruption, for at least 28 days prior to starting the investigational product, during the study (including dose interruptions), and for 16 weeks (112 days) after discontinuation of study treatment;
    • Refrain from breastfeeding a child or donating blood, eggs, or ovum for the duration of the study and for at least 16 weeks (112 days) after the last dose of study treatment.
  • Male participants must:
    • Agree to use a condom, defined as a male latex condom or nonlatex condom NOT made out of natural (animal) membrane (e.g., polyurethane), during sexual contact with a pregnant female or a female of childbearing potential while participating in the study, during dose interruptions and for at least 16 weeks (112 days) following investigational product discontinuation, even if he has undergone a successful vasectomy;
    • Refrain from donating blood or sperm for the duration of the study and for 16 weeks (112 days) after the last dose of study treatment.
  • Ability to adhere to study visit schedule and understand and comply with all protocol requirements.
  • Ability to understand and provide written informed consent.

Exclusion Criteria:

  • Diagnosis of pulmonary hypertension WHO Groups 2, 3, 4, or 5.
  • Diagnosis of the following PAH Group 1 subtypes: human immunodeficiency virus (HIV)-associated PAH and PAH associated with portal hypertension. Exclusions in PAH Group I should also include schistosomiasis APAH and pulmonary veno-occlusive disease.
  • Hemoglobin (Hgb) at screening above gender-specific upper limit of normal (ULN), per local laboratory test.
  • Baseline platelet count < 50,000/mm^3 (< 50.0 × 10^9/L) at screening.
  • Uncontrolled systemic hypertension as evidenced by sitting systolic blood pressure> 160 mmHg or sitting diastolic blood pressure > 100 mmHg during screening visit after a period of rest.
  • Baseline systolic BP < 90 mmHg at screening.
  • Pregnant or breastfeeding women.
  • Any of the following clinical laboratory values at the screening visit:
    • Estimated glomerular filtration rate (eGFR) < 30 mL/min/m^2 (as defined by the Modification of Diet in Renal Disease [MDRD] equation);
    • Serum alanine aminotransferase (ALT), aspartate aminotransferase (AST), or total bilirubin levels > 3 × ULN (bilirubin criterion waived if there is a documented history of Gilbert’s syndrome).
  • Any of the following clinical laboratory values at the screening visit:
    • Estimated glomerular filtration rate (eGFR) < 30 mL/min/m^2 (as defined by MDRD equation);
    • Serum alanine aminotransferase or aspartate aminotransferase levels > 3 x ULN or total bilirubin > 1.5 x ULN.
  • Currently enrolled in or have completed any other investigational product study within 30 days for small-molecule drugs or within 5 half-lives for biologics prior to the date of signed informed consent.
  • Prior exposure to sotatercept (ACE-011) or luspatercept (ACE-536) and/or excipients or known allergic reaction to either one.
  • Have history of full or partial pneumonectomy.
  • Pulmonary function test (PFT) values of forced vital capacity (FVC) < 60% predicted at the screening visit or within 6 months prior to the screening visit. If PFT is not available, a chest CT scan showing more than mild interstitial lung disease at the screening visit or 1 year prior to it.
  • 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).
  • History of more than mild obstructive sleep apnea that is untreated.
  • Known history of portal hypertension or chronic liver disease, including hepatitis B and/or hepatitis C (with evidence of recent infection and/or active virus replication) defined as mild to severe hepatic impairment (Child-Pugh Class A-C).
  • History of restrictive, constrictive or congestive cardiomyopathy.
  • History of atrial septostomy within 180 days prior to the screening visit.
  • Electrocardiogram (ECG) with Fridericia's corrected QT interval (QTcF) > 500 ms during the screening period.
  • Personal or family history oflong QT syndrome (LQTS) or sudden cardiac death.
  • Left ventricular ejection fraction < 45% on historical echocardiogram within 6 months prior to the screening visit or pulmonary capillary wedge pressure > 15 mmHg as determined in the Screening Period RHC.
  • Any symptomatic coronary disease events within 6 months (prior myocardial infarction, percutaneous coronary interventi on, coronary artery bypass graft surgery, or cardiac anginal chest pain) within 6 months of the screening visit.
    • Note: Anginal pain can be ignored as an exclusion criterion if coronary angiography shows no obstructions.
  • Cerebrovascular accident within 3 months prior to the screening visit.
  • Acutely decompensated heart failure within 30 days prior to the screening visit, as per investigator assessment.
  • Significant (2: 2+ regurgitation) mitral regurgitation or aortic regurgitation valvular disease, mitral stenosis and more than mild aortic valve stenosis.
  • Received intravenous inotropes (e.g., dobutamine, dopamine, norepinephrine, vasopressin) within 30 days prior to the screening visit.

Eligibility last updated 5/18/22. Questions regarding updates should be directed to the study team contact.

Participating Mayo Clinic locations

Study statuses change often. Please contact the study team for the most up-to-date information regarding possible participation.

Mayo Clinic Location Status Contact

Jacksonville, Fla.

Mayo Clinic principal investigator

Charles Burger, M.D.

Closed for enrollment

Contact information:

Caroline Chang

Chang.Caroline@mayo.edu

Rochester, Minn.

Mayo Clinic principal investigator

Charles Burger, M.D.

Closed for enrollment

Contact information:

Louise Durst R.N.

(507) 284-1838

durst.louise@mayo.edu

More information

Publications

Publications are currently not available