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
Sites (24)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| Hopital Erasme Coordinator of this site? Confirm its status | Anderlecht | Belgium | Completed |
| UZ Leuven Coordinator of this site? Confirm its status | Leuven | Belgium | Completed |
| Universitaetsklinikum Carl Gustav Carus Dresden an der Technischen Universitaet Dresden AöR Coordinator of this site? Confirm its status | Dresden | Germany | Completed |
| Universityclinic Giessen And Marburg GmbH Coordinator of this site? Confirm its status | Giessen | Germany | Completed |
| Medizinische Hochschule Hannover Service GmbH Coordinator of this site? Confirm its status | Hanover | Germany | Completed |
| Thoraxklinik At University Of Heidelberg Coordinator of this site? Confirm its status | Heidelberg | Germany | Completed |
| University of Leipzig Coordinator of this site? Confirm its status | Leipzig | Germany | Completed |
| Klinikum Würzburg Mitte gGmbH Standort Missioklinik Coordinator of this site? Confirm its status | Würzburg | Germany | Completed |
| Centre Hospitalier Regional Et Universitaire De Brest Coordinator of this site? Confirm its status | Brest Cedex 2 | France | Completed |
| Assistance Publique Hopitaux De Paris Coordinator of this site? Confirm its status | Le Kremlin-Bicetre | France | Completed |
| Centre Hospitalier Universitaire De Lille Coordinator of this site? Confirm its status | Lille Cedex | France | Completed |
| CHU De Rouen Coordinator of this site? Confirm its status | Rouen Cedex | France | Completed |
| Centre Hospitalier Universitaire de Toulouse Coordinator of this site? Confirm its status | Toulouse | France | Completed |
| University General Hospital of Thessaloniki - AHEPA Coordinator of this site? Confirm its status | Thessaloniki | Greece | Completed |
| Centro Cardiologico Monzino S.p.A. Coordinator of this site? Confirm its status | Milan | Italy | Completed |
| Fondazione IRCCS San Gerardo dei Tintori Coordinator of this site? Confirm its status | Monza | Italy | Completed |
| Università degli studi di Napoli Federico II Coordinator of this site? Confirm its status | Naples | Italy | Completed |
| Fondazione IRCCS Policlinico San Matteo Coordinator of this site? Confirm its status | Pavia | Italy | Completed |
| Azienda Ospealiero Universitaria Policlinico Umberto I Coordinator of this site? Confirm its status | Rome | Italy | Completed |
| Krakowski Szpital Specjalistyczny Im. Jana Pawla II Coordinator of this site? Confirm its status | Cracow | Poland | Completed |
| Samodzielny Publiczny Szpital Kliniczny Nr 4 w Lublinie Coordinator of this site? Confirm its status | Lublin | Poland | Completed |
| Specjalistyczny Szpital Im. Dra Alfreda Sokolowskiego Coordinator of this site? Confirm its status | Walbrzych | Poland | Completed |
| Sahlgrenska University Hospital-Vastra Gotalandsregionen Coordinator of this site? Confirm its status | Goteborg | Sweden | Completed |
| Uppsala University Hospital Coordinator of this site? Confirm its status | Uppsala | Sweden | Completed |
This page is information, not medical advice. Discuss any trial with your doctor.