- ICH GCP
- Registre américain des essais cliniques
- Essai clinique NCT07740421
A Prospective, Multicenter, Phase III Clinical Evaluation of the Safety and Efficacy of NH002 as a Contrast Agent Administrated Via Intravenous Bolus Injection and Infusion for Subjects Undergoing Cardiac Echocardiography
28 juillet 2026 mis à jour par: Trust Bio-sonics, Inc.
This is a phase III, prospective, multicenter, open-label, crossover study of the safety and efficacy of NH002-enhanced echocardiography in adult subjects with suboptimal images on non-contrast 2D transthoracic echocardiography with harmonic imaging within 30 days ahead of NH002 administration.
The efficacy for two different modes of administration (i.e., IV bolus injection and infusion) will be evaluated independently.
Aperçu de l'étude
Statut
Pas encore de recrutement
Les conditions
Intervention / Traitement
Type d'étude
Interventionnel
Inscription (Estimé)
150
Phase
- Phase 3
Critères de participation
Les chercheurs recherchent des personnes qui correspondent à une certaine description, appelée critères d'éligibilité. Certains exemples de ces critères sont l'état de santé général d'une personne ou des traitements antérieurs.
Critère d'éligibilité
Âges éligibles pour étudier
- Adulte
- Adulte plus âgé
Accepte les volontaires sains
Non
La description
Inclusion Criteria:
- 18 years of age or older
- Ability to understand and the willingness to provide written informed consent
- Having or suspected of having cardiac disease
- Undergone a transthoracic echo within 30 days prior to NH002 dose administration, resulting in suboptimal LVEBD, as defined by 2 or more segments of 6 segments of the ventricular border that cannot be visualized reliably in any of the standard apical 4-, 2-, and 3-chamber views during the resting non-contrast ultrasound examination
Exclusion Criteria:
Any evidence of other severe or unstable cardiopulmonary and/or systemic hemodynamic conditions deemed unsuitable for the study by the investigator(s) prior to NH002 dose administration, including, but not limited to:
- ongoing or recent acute coronary syndrome within 6 months
- uncontrolled serious ventricular arrhythmias
- decompensated or inadequately controlled congestive heart failure (New York Heart Association Class IV)
- atrial fibrillation or current uncontrolled cardiac arrhythmias causing symptoms or hemodynamic compromise
- uncontrolled hypertension (i.e., resting systolic blood pressure >200 mmHg, diastolic blood pressure >110 mmHg, or arterial hypotension [defined as systolic blood pressure ≤ 90 mmHg])
- acute aortic dissection
- Known or suspected hypersensitivity to one or more of the ingredients of NH002, perflutren, Definity, or other echocardiographic contrast agents
- Known or suspected hypersensitivity to PEG, prior reactions to common PEG-containing products such as colonoscopy bowel preparations, and certain laxatives (e.g., Miralax)
- Received an investigational compound within 30 days before enrolling in the study
- Received any contrast agent either intravascularly or orally within 48 hours prior to NH002 dose administration
Pregnant or lactating female. Exclude the possibility of pregnancy:
- testing on-site at the institution (serum or urine β-human chorionic gonadotropin) within 7 days prior to the start of NH002 dose administration, and
- history of using an adequate and medically approved method of contraception to avoid pregnancy for at least 1 month prior to NH002 dose administration and willing to continue using the same method for the duration of the study, or
- surgical history (e.g., tubal ligation or hysterectomy), or
- postmenopausal with a minimum of 1 year without menses.
- Serious medical or psychiatric illness/condition likely, in the judgment of the investigator, to interfere with compliance with protocol treatment/research
Plan d'étude
Cette section fournit des détails sur le plan d'étude, y compris la façon dont l'étude est conçue et ce que l'étude mesure.
Comment l'étude est-elle conçue ?
Détails de conception
- Objectif principal: Diagnostique
- Répartition: Randomisé
- Modèle interventionnel: Affectation croisée
- Masquage: Aucun (étiquette ouverte)
Armes et Interventions
Groupe de participants / Bras |
Intervention / Traitement |
|---|---|
|
Expérimental: Sequence 1
Subjects who are enrolled in the study will undergo two-time resting unenhanced ultrasound examination (shortly before each dose of NH002 administration) and two-time NH002 contrast-enhanced examination on the same day at Day 1 (with the first administration via bolus injection and the second via infusion), with the standard apical 4-, 2-, and 3-chamber views obtained with B-mode and contrast-specific imaging, respectively.
|
NH002 est formulé sous forme de suspension injectable de microbulles pour administration intraveineuse.
NH002 nécessite un processus d'activation avant utilisation.
|
|
Expérimental: Sequence 2
Subjects who are enrolled in the study will undergo two-time resting unenhanced ultrasound examination (shortly before each dose of NH002 administration) and two-time NH002 contrast-enhanced examination on the same day at Day 1 (with the first administration via infusion and the second via bolus injection), with the standard apical 4-, 2-, and 3-chamber views obtained with B-mode and contrast-specific imaging, respectively.
|
NH002 est formulé sous forme de suspension injectable de microbulles pour administration intraveineuse.
NH002 nécessite un processus d'activation avant utilisation.
|
Que mesure l'étude ?
Principaux critères de jugement
Mesure des résultats |
Description de la mesure |
Délai |
|---|---|---|
|
Left Ventricular Endocardial Border Delineation (LVEBD)
Délai: Image data obtained pre-injection and within 15 minutes post-injection
|
The first primary efficacy endpoint will be the change from baseline (prior to each dose of NH002 administration) in total LVEBD scores (UEUS vs CEUS) defined using a 16-segment model derived from the standard 17-segment model, as assessed through blinded central reading.
The LV endocardium of the standard apical 4-, 2-, and 3-chamber views is divided into 6 segments, with 2 basal, mid-, and apical segments in each view, of which 2 segments are shared in the standard apical 4- and 3-chamber views (i.e., a total of 16 segments in the 3 views).
The 17th segment at the apex will not be scored since it does not connect to any part of the LV endocardial border.
For each segment, LVEBD is graded as follows: 0 = inadequate border (border not visible); 1 = sufficient (border barely visible); 2 = good (border clearly visible).
A total delineation score (0 to 32) is obtained by adding the scores from a total of the 16 segments in the 3 views.
|
Image data obtained pre-injection and within 15 minutes post-injection
|
|
Left Ventricular Opacification (LVO)
Délai: Image data obtained pre-injection and within 15 minutes post-injection
|
The co-primary endpoint will be the proportion of subjects with adequate LVO defined by an LVO grade of +2 (moderate) or +3 (complete), as assessed through blinded central reading.
|
Image data obtained pre-injection and within 15 minutes post-injection
|
Mesures de résultats secondaires
Mesure des résultats |
Description de la mesure |
Délai |
|---|---|---|
|
The number and percentage of subjects with suboptimal echocardiography converted into optimal echocardiography
Délai: Image data obtained pre-injection and within 15 minutes post-injection
|
Objective evaluation of the number and percentage of subjects with suboptimal echocardiography (based on the definition of inadequate LVEBD, i.e., at least two segments [in any chamber view] with an LVEBD score of 0) converted into optimal echocardiography following administration of study drug will be summarized for each reader.
|
Image data obtained pre-injection and within 15 minutes post-injection
|
|
Standard 12-lead ECGs
Délai: From pre-injection (before the first dose) to 24 hours (after the end of second dose)
|
Standard 12-lead ECGs assessed prior to injection and at 10 and 30 minutes after the initiation of IV bolus injection and infusion; and at 24 hours after the end of the second dose of NH002
|
From pre-injection (before the first dose) to 24 hours (after the end of second dose)
|
|
Blood Pressure (BP)
Délai: From pre-injection (before the first dose) to 24 hours (after the end of second dose)
|
Change in BP assessed prior to injection and at 5, 10 and 30 minutes after the initiation of IV bolus injection and infusion; and at 24 hours after the end of the second dose of NH002
|
From pre-injection (before the first dose) to 24 hours (after the end of second dose)
|
|
Heart Rate (HR)
Délai: From pre-injection (before the first dose) to 24 hours (after the end of second dose)
|
Change in HR assessed prior to injection and at 5, 10 and 30 minutes after the initiation of IV bolus injection and infusion; and at 24 hours after the end of the second dose of NH002
|
From pre-injection (before the first dose) to 24 hours (after the end of second dose)
|
|
SpO2
Délai: From pre-injection (before the first dose) to 24 hours (after the end of second dose)
|
SpO2 assessed by pulse oximetry prior to injection and at 5, 10 and 30 minutes after the initiation of IV bolus injection and infusion; and at 24 hours after the end of the second dose of NH002
|
From pre-injection (before the first dose) to 24 hours (after the end of second dose)
|
|
Physical Examination (PE)
Délai: From pre-injection (before the first dose) to 24 hours (after the end of second dose)
|
PE assessed prior to injection and at 30 minutes after the initiation of IV bolus injection and infusion; and at 24 hours after the end of the second dose of NH002
|
From pre-injection (before the first dose) to 24 hours (after the end of second dose)
|
|
Adverse Events (AEs)
Délai: From pre-injection (before the first dose) to 24 hours (after the end of second dose)
|
AEs assessed prior to injection and at 5, 10, 15 and 30 minutes after the initiation of IV bolus injection and infusion; and at 24 hours after the end of the second dose of NH002
|
From pre-injection (before the first dose) to 24 hours (after the end of second dose)
|
Collaborateurs et enquêteurs
C'est ici que vous trouverez les personnes et les organisations impliquées dans cette étude.
Parrainer
Collaborateurs
Dates d'enregistrement des études
Ces dates suivent la progression des dossiers d'étude et des soumissions de résultats sommaires à ClinicalTrials.gov. Les dossiers d'étude et les résultats rapportés sont examinés par la Bibliothèque nationale de médecine (NLM) pour s'assurer qu'ils répondent à des normes de contrôle de qualité spécifiques avant d'être publiés sur le site Web public.
Dates principales de l'étude
Début de l'étude (Estimé)
1 juillet 2026
Achèvement primaire (Estimé)
1 juillet 2027
Achèvement de l'étude (Estimé)
1 juillet 2027
Dates d'inscription aux études
Première soumission
28 juillet 2026
Première soumission répondant aux critères de contrôle qualité
28 juillet 2026
Première publication (Réel)
31 juillet 2026
Mises à jour des dossiers d'étude
Dernière mise à jour publiée (Réel)
31 juillet 2026
Dernière mise à jour soumise répondant aux critères de contrôle qualité
28 juillet 2026
Dernière vérification
1 juillet 2026
Plus d'information
Termes liés à cette étude
Mots clés
Termes MeSH pertinents supplémentaires
Autres numéros d'identification d'étude
- NH002-LV-03
Plan pour les données individuelles des participants (IPD)
Prévoyez-vous de partager les données individuelles des participants (DPI) ?
NON
Informations sur les médicaments et les dispositifs, documents d'étude
Étudie un produit pharmaceutique réglementé par la FDA américaine
Oui
Étudie un produit d'appareil réglementé par la FDA américaine
Non
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