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NCT04732221CompletedPhase 2/3

A Study of the Efficacy and Safety of MK-5475 in Participants with Pulmonary Arterial Hypertension

A Phase 2/3, Multicenter, Randomized, Double-blind, Placebo-Controlled, Adaptive Design Study to Evaluate the Efficacy and Safety of MK-5475 in Adults with Pulmonary Arterial Hypertension

Source: EU CTIS (euclinicaltrials.eu) · Last updated 8 Apr 2024

Brief summary (registry, in English)

1. To evaluate the effect of MK-5475 versus placebo on the pulmonary vascular resistance (PVR) at Week 12 in the Phase 2 Cohort 2. To evaluate the effect of MK-5475 versus placebo on 6-minute walk distance (6MWD) at Week 12 in the Phase 3 Cohort

Status (registry)
Completed
Phase (registry)
Phase 2/3
Study type
Interventional
Enrollment
68 (actual)
First submitted
17 Mar 2023
Start date
25 Jun 2021
Lead sponsor
Merck Sharp & Dohme LLC
NCT number
NCT04732221
EU CT number
2022-500877-15-00
EudraCT number
2020-001108-40

What you commit to

  • Study type: Interventional · Phase 2/3
  • Participants enrolled: 68
  • 24 sites in 7 countries
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of EU CTIS (euclinicaltrials.eu). It describes the study, not your situation.

Who cannot take part

Copied verbatim from EU CTIS (euclinicaltrials.eu) and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Oxygen saturation measured by pulse oximetry (SpO₂) <90%, despite supplemental oxygen therapy.

Other illness

  • Group 2 to 5 pulmonary hypertension
  • History of cancer, except: nonmelanomatous skin carcinoma or carcinoma in situ of the cervix or other malignancies which have been successfully treated, with appropriate follow up, and unlikely to recur for the duration of the study.
  • Evidence of more-than-mild obstructive lung disease or parenchymal lung disease.

Lab values

  • PAH in one of the following groups: Long term responders to calcium channel blockers, or overt features of venous/capillary involvement
  • Evidence or history of left heart disease, including any of the following: Left ventricular ejection fraction (LVEF) ≤45%, moderate or severe left-sided valvular disease (aortic or mitral valve stenosis or regurgitation), or significant left ventricular diastolic dysfunction on echocardiographic evaluation.
  • Presence of 3 or more of the following risk factors for heart failure with preserved ejection fraction: BMI>30 kg/m², essential systemic hypertension, diabetes mellitus of any type, or coronary artery disease.
  • Chronic renal insufficiency (eGFR <30 mL/min)
  • Chronic liver disease (i.e., Child-Pugh B or C), portal hypertension, cirrhosis, or significant hepatic laboratory abnormalities.

Other

  • Current smoker or currently uses electronic cigarettes (vapes).
  • Evidence of more-than-mild obstructive sleep apnea (OSA) that is untreated.

Who the study is looking for

  • Pulmonary arterial hypertension (PAH) in one of the following groups: Idiopathic PAH, heritable PAH, drug and toxin-induced PAH, PAH associated with connective tissue disease, HIV infection, or congenital heart disease
  • Diagnosis of PAH documented by right heart catheterization (RHC).
  • Eligibility RHC meeting all of the following criteria: Mean pulmonary artery pressure (mPAP) ≥25 mmHg, pulmonary vascular resistance (PVR) of ≥3 Wood units, and pulmonary capillary wedge pressure (PCWP) or left ventricular end diastolic pressure (LVEDP) ≤15 mmHg.
  • World Health Organization functional class (WHO-FC) symptoms between Class II and IV.
  • Two 6-Minute walk distance (6MWD) measurements between 150 and 500 meters, one at screening and one at randomization.
  • Stable concomitant background PAH-specific therapy.
  • Body Mass Index (BMI) between 18.5 kg/m² and 40 kg/m².

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on EU CTIS (euclinicaltrials.eu)

Sites (24)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Hopital Erasme
Coordinator of this site? Confirm its status
AnderlechtBelgiumCompleted
UZ Leuven
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LeuvenBelgiumCompleted
Universitaetsklinikum Carl Gustav Carus Dresden an der Technischen Universitaet Dresden AöR
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DresdenGermanyCompleted
Universityclinic Giessen And Marburg GmbH
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GiessenGermanyCompleted
Medizinische Hochschule Hannover Service GmbH
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HanoverGermanyCompleted
Thoraxklinik At University Of Heidelberg
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HeidelbergGermanyCompleted
University of Leipzig
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LeipzigGermanyCompleted
Klinikum Würzburg Mitte gGmbH Standort Missioklinik
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WürzburgGermanyCompleted
Centre Hospitalier Regional Et Universitaire De Brest
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Brest Cedex 2FranceCompleted
Assistance Publique Hopitaux De Paris
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Le Kremlin-BicetreFranceCompleted
Centre Hospitalier Universitaire De Lille
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Lille CedexFranceCompleted
CHU De Rouen
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Rouen CedexFranceCompleted
Centre Hospitalier Universitaire de Toulouse
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ToulouseFranceCompleted
University General Hospital of Thessaloniki - AHEPA
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ThessalonikiGreeceCompleted
Centro Cardiologico Monzino S.p.A.
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MilanItalyCompleted
Fondazione IRCCS San Gerardo dei Tintori
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MonzaItalyCompleted
Università degli studi di Napoli Federico II
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NaplesItalyCompleted
Fondazione IRCCS Policlinico San Matteo
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PaviaItalyCompleted
Azienda Ospealiero Universitaria Policlinico Umberto I
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RomeItalyCompleted
Krakowski Szpital Specjalistyczny Im. Jana Pawla II
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CracowPolandCompleted
Samodzielny Publiczny Szpital Kliniczny Nr 4 w Lublinie
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LublinPolandCompleted
Specjalistyczny Szpital Im. Dra Alfreda Sokolowskiego
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WalbrzychPolandCompleted
Sahlgrenska University Hospital-Vastra Gotalandsregionen
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GoteborgSwedenCompleted
Uppsala University Hospital
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UppsalaSwedenCompleted

This page is information, not medical advice. Discuss any trial with your doctor.