MedPath

A Study of Selexipag as Add-On Treatment to Standard of Care in Children With Pulmonary Arterial Hypertension

Phase 3
Active, not recruiting
Conditions
Hypertension, Pulmonary
Interventions
Drug: Placebo
Registration Number
NCT04175600
Lead Sponsor
Actelion
Brief Summary

The purpose of this study is to evaluate whether the addition of selexipag to standard of care treatment delays disease progression in children with Pulmonary Arterial Hypertension (PAH) in comparison to placebo.

Detailed Description

Pediatric PAH is a rare and progressive disorder associated with considerable morbidity and mortality. Given the significant medical need to develop treatments in children with PAH, further clinical studies in the pediatric population are therefore needed to provide more data for the management of PAH in children. Selexipag (JNJ-67896049) is an orally available, selective, and long-acting non-prostanoid agonist of the prostacyclin receptor approved and commercially available for the treatment of adult participants with PAH. Selexipag and its metabolite possess anti-fibrotic, anti-proliferative, and anti-thrombotic properties. Currently, no medicines targeting prostacyclin pathway are approved for pediatric use in PAH. An effective and orally available therapy acting on the prostacyclin receptor such as selexipag introduced at medically appropriate stage of PAH disease, and primarily in combination with current first-line oral PAH-specific medicines in participants in need of additional therapy because of insufficient disease control would represents a major advance to the therapeutic management of PAH pediatric participants. This study consists of a screening period of up to 6 weeks and a double-blind treatment period, including up-titration and maintenance periods, followed by a 3-year open-label extension period (OLEP) and a 30-day safety follow-up period that occurs after the last dose of study intervention (either double-blind or open-label). Safety, pharmacokinetic and efficacy assessments will be performed during the study. An Independent Data Monitoring Committee (IDMC) will be established to monitor data on an ongoing basis, to review interim data, and to ensure the continuing safety of the participants enrolled in this study. The approximate duration of the study is 8 years.

Recruitment & Eligibility

Status
ACTIVE_NOT_RECRUITING
Sex
All
Target Recruitment
138
Inclusion Criteria
  • Participants between greater than or equal to (>=) 2 and less than (<) 18 years of age weighing >=9 kilogram (kg) at randomization
  • Pulmonary arterial hypertension (PAH) diagnosis confirmed by documented historical right heart catheterization (RHC) performed at any time before participant's screening
  • PAH (World Health Organization [WHO] Group 1), including participants with Down syndrome, of the following etiologies: Idiopathic PAH (IPAH); Heritable PAH (HPAH); PAH associated with congenital heart disease (PAH-associated with congenital heart disease [aCHD]) (PAH with coincidental CHD [that is, a small atrial septal defect, ventricular septal defect, or patent ductus arteriosus that does not itself account for the development of elevated PVR] and if approved by the BCAC) and Post-operative PAH (persisting / recurring/ developing >=6 months after repair of CHD); Drug or toxin-induced; PAH associated with Human immunodeficiency virus (HIV)
  • WHO functional class (FC) II and III
  • Participants treated with at least 1 PAH-specific treatment, example, an Endothelin receptor antagonist (ERA) and/or a Phosphodiesterase type-5 (PDE-5) inhibitor/soluble guanylate cyclase stimulator, provided that the treatment dose(s) has been stable for at least 3 months prior to first dose of study intervention
Exclusion Criteria
  • PAH due to portal hypertension, schistosomiasis, pulmonary veno-occlusive disease, and/or pulmonary capillary hemangiomatosis
  • PAH associated with Eisenmenger syndrome
  • Previous exposure to Uptravi (selexipag)
  • Known concomitant life-threatening disease with a life expectancy <12 months
  • Pregnant, planning to become pregnant, or lactating
  • Known allergies, hypersensitivity, or intolerance to selexipag or its excipients

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
SelexipagSelexipagParticipants will receive selexipag based on the body weight on Day 1 and will continue thereafter with twice daily dosing. Selexipag will be uptitrated during the first 12 weeks until the participants reaches the individual maximum tolerated dose (iMTD) or until a maximum dose corresponding to their baseline body-weight category is achieved. Uptitration is followed by a maintenance period after Week 12 until end of treatment (EOT), at the maximum tolerated dose.
PlaceboPlaceboParticipants will receive matching placebo based on the body weight on Day 1 and will continue thereafter with twice daily dosing.
Primary Outcome Measures
NameTimeMethod
Time to Disease ProgressionFrom randomization up to 7 days after study treatment discontinuation (up to 5 years)

Time to disease progression is the time from randomization up to 7 days after study treatment discontinuation. Disease progression is defined as the first occurrence of either of the following components: Death (all causes), Atrial septostomy or Potts' anastomosis, or registration on lung transplant list, Hospitalization due to worsening pulmonary arterial hypertension (PAH), Clinical worsening of PAH.

Secondary Outcome Measures
NameTimeMethod
Change from Baseline in Systolic and Diastolic Arterial Blood PressureBaseline up to end of treatment (EOT) (up to 8 years)

Change from baseline in systolic and diastolic arterial blood pressure to all assessed time points will be reported.

Change from Baseline in Pulse RateBaseline up to EOT (up to 8 years)

Change from baseline in pulse rate to all assessed time points will be reported.

Change from Baseline in Body WeightBaseline up to EOT (up to 8 years)

Change from baseline in body weight to all assessed time points will be reported.

Change from Baseline in HeightBaseline up to EOT (up to 8 years)

Change from baseline in height to all assessed time points will be reported.

Sexual Maturation (Tanner Stage) Change from Baseline to all Assessed Time PointsUp to 3 days after study treatment discontinuation (up to EOT) (multiple timepoints up to 8 years)

The sexual maturation change as per Tanner stage will be assessed from baseline to all assessed time points. Tanner stage I is defined as no pubic hair at all (prepubertal Dominic state); stage II is defined as a small amount of long, downy hair with slight pigmentation at the base of the penis and scrotum (males) or on the labia majora (females); stage III is defined as when the hair becomes more coarse and curly, and begins to extend laterally; stage IV is defined as adult-like hair quality, extending across pubis but sparing medial thighs; and stage V is defined as when the: hair extends to medial surface of the thighs.

Percentage of Participants with Treatment-emergent Marked Laboratory AbnormalitiesBaseline up to EOT (up to 8 years)

Percentage of participants with treatment-emergent marked laboratory (serum chemistry \[including pregnancy testing and thyroid markers\] and hematology) abnormalities will be reported.

Treatment-emergent Change from Baseline in Thyroid Stimulating HormoneBaseline up to EOT (up to 8 years)

Treatment-emergent change from baseline in thyroid stimulating hormone over time will be reported.

Time to First Clinical Event Committee (CEC)-confirmed Hospitalization or Death for PAHUntil 7 days after study treatment discontinuation (Up to 8 years)

Time to first CEC-confirmed hospitalization or death for PAH is the time (days) from randomization to first occurrence of CEC-confirmed hospitalization for PAH or death due to PAH up to 7 days after study intervention discontinuation.

Trough Plasma Concentration at Steady-state (Ctrough,ss) of Selexipag and its Metabolite ACT-333679Weeks 16, 24 and every 12 weeks thereafter (up to 8 years)

Ctrough,ss is defined as the plasma concentration just prior to the morning dose, with the last study intervention administration one day prior to the pharmacokinetic sampling and will be reported for Selexipag and its metabolite ACT-333679.

Change from Baseline at Week 24 in Log2 N-terminal Pro-brain Natriuretic Peptide (NT-proBNP)Baseline up to Week 24

The change from baseline at week 24 in log2 NT-proBNP will be reported.

Percentage of Participants with Treatment-emergent Electrocardiogram AbnormalitiesBaseline up to EOT (up to 8 years)

Percentage of participants with treatment-emergent electrocardiogram abnormalities will be reported.

Percentage of Participants with Treatment-emergent Adverse Events (TEAEs) and Serious AEsUp to 5 years

An adverse event (AE) is any untoward medical event that occurs in a participant administered an investigational product, and it does not necessarily indicate only events with clear causal relationship with the relevant investigational product. TEAEs are AEs with onset during the intervention period or that are a consequence of a pre-existing condition that has worsened since baseline. A SAE is an AE resulting in any of the following outcomes or deemed significant for any other reason: death; initial or prolonged inpatient hospitalization; life-threatening experience (immediate risk of dying); persistent or significant disability/incapacity; congenital anomaly.

Percentage of Participants with AEs Leading to Premature Discontinuation of Study TreatmentUp to 5 years

Percentage of participants with AEs leading to premature discontinuation of study treatment will be reported.

Trial Locations

Locations (114)

Szpital Kliniczny im Karola Jonschera

🇵🇱

Poznan, Poland

Phoenix Children's Hospital

🇺🇸

Phoenix, Arizona, United States

UCLA Medical Center

🇺🇸

Los Angeles, California, United States

UCSF

🇺🇸

San Francisco, California, United States

Childrens Hospital Colorado

🇺🇸

Aurora, Colorado, United States

Children's National Medical Center

🇺🇸

Washington, District of Columbia, United States

Congenital Heart Center of the University of Florida

🇺🇸

Gainesville, Florida, United States

Riley Hospital for Children

🇺🇸

Indianapolis, Indiana, United States

Detroit Medical Center

🇺🇸

Detroit, Michigan, United States

Cincinnati Children's Hospital Medical Center

🇺🇸

Cincinnati, Ohio, United States

Scroll for more (104 remaining)
Szpital Kliniczny im Karola Jonschera
🇵🇱Poznan, Poland

MedPath

Empowering clinical research with data-driven insights and AI-powered tools.

© 2025 MedPath, Inc. All rights reserved.