Study to Evaluate Sotatercept (MK-7962) in Children With Pulmonary Arterial Hypertension (PAH) (MK-7962-008)

Launched by MERCK SHARP & DOHME LLC · Oct 17, 2022

Keywords

ClinConnect Summary

This clinical trial is studying a medication called sotatercept to see how safe it is and how well it works in children aged 1 to 17 years who have Pulmonary Arterial Hypertension (PAH). PAH is a condition that affects the blood vessels in the lungs, making it hard for blood to flow and causing increased pressure. The study will last for 24 weeks and is looking for children who have been diagnosed with PAH and are currently receiving standard treatments.

To be eligible for the trial, children must have a confirmed diagnosis of PAH from a specific test done in the past and must be on stable treatment for their condition. The trial is open to all genders and is currently recruiting participants. If your child is selected to participate, they will receive sotatercept and will be closely monitored for any side effects or changes in their health. It's important to know that there are specific guidelines about pregnancy and contraception for both male and female participants during the study period. This trial aims to provide valuable information about treating PAH in children, which could help improve future treatments.

Gender

ALL

Eligibility criteria

• • Inclusion Criteria
• * Documented, historic diagnostic right heart catheterization (RHC) any time before Screening confirming the diagnosis of PAH WHO Group 1 in any of the following subtypes:
• • Idiopathic pulmonary arterial hypertension (IPAH)
• • Heritable PAH
• • Drug/toxin-induced PAH
• • PAH associated with connective tissue disease
• • PAH-congenital heart disease (CHD) with shunt closure \>6 months before Screening and subsequently confirmed by RHC before Screening
• • PAH with coincidental shunt.
• • Must be on a stable dose(s) of background PAH therapy (phosphdiesterase-5 (PDE5) inhibitors, endothelin receptor antagonists (ERAs), soluble guanylate cyclase stimulators (sGCS), or prostanoids \[including subcutaneous and intravenous\])
• * If male, agree to the following during the intervention period and for at least 16 weeks (112 days) after the last dose of study intervention:
• • Abstains from heterosexual intercourse as their preferred and usual lifestyle (abstinent on a long-term and persistent basis) and agrees to remain abstinent or
• * Uses contraception unless confirmed to be azoospermic (vasectomized or secondary to medical cause, documented from the site personnel's review of the participant's medical records, medical examination, or medical history interview) as detailed below:
• • Uses a male condom plus partner use of an additional contraceptive method when having penile-vaginal intercourse with a woman of childbearing potential (WOCBP) who is not currently pregnant Note: Men with a pregnant or breastfeeding partner must agree to remain abstinent from penile-vaginal intercourse or use a male condom during each episode of penile-vaginal penetration.
• • If female, must be either not a WOCBP or use a contraceptive method that is highly effective or be abstinent from heterosexual intercourse during the intervention period and for at least 16 weeks (112 days) after the last dose of study intervention
• • If male, agrees to refrain from donating blood or sperm for the duration of the study and for 16 weeks (112 days) after the last dose of study intervention
• • If female, agrees to refrain from 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 intervention
• • Exclusion Criteria
• • History of left-sided heart disease, including valvular disease (eg, moderate or greater mitral or aortic regurgitation or stenosis), left ventricular outflow tract obstruction, and/or left heart failure (eg, restrictive or dilated cardiomyopathy)
• • Severe (as based on the opinion of the investigator) congenital or developmental abnormalities of the lung, thorax, and/or diaphragm
• • History of Eisenmenger syndrome, Potts shunt, or atrial septostomy
• • Unrepaired or residual cardiac shunt
• • Diagnosis of pulmonary veno-occlusive diseases, pulmonary capillary hemangiomatosis, or overt signs of capillary and/or venous involvement
• • PAH associated with portal hypertension
• • Known visceral (lung, liver, or brain) arteriovenous malformation(s)
• • History of full or partial pneumonectomy
• • Untreated more than mild obstructive sleep apnea
• • History of known pericardial constriction
• • Family history of sudden cardiac death or long QT syndrome
• • Any current or prior history of symptomatic coronary disease (myocardial infarction, percutaneous coronary intervention, coronary artery bypass graft surgery, or cardiac anginal chest pain) within 6 months before Screening
• • Cerebrovascular accident within 3 months before Screening
• • Prior exposure to sotatercept or luspatercept or has had an allergic reaction to any of their excipients