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Open-label Extension Study of Enlicitide Decanoate (MK-0616/Enlicitide Oral PCSK9 Inhibitor) in Adults With Hypercholesterolemia (MK-0616-019) CORALreef Extension

Hypercholesterolemia

This is an extension study to evaluate the longer-term safety and efficacy of enlicitide decanoate in adults with hypercholesterolemia who completed either study MK-0616-013 (NCT05952856), study MK-0616-017 (NCT05952869), or study MK-0616-018 (NCT06450366).

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Conditions de participation

  • Sexe:

    ALL
  • Âges admissibles:

    18 and up

Critères de participation

Inclusion Criteria:

* Has completed an enlicitide decanoate (also known as enlictide and MK-0616) parent study \[MK-0616-013 (NCT05952856), MK-0616-017 (NCT05952869), and MK-0616-018 (NCT06450366)\] per protocol (including the final assessments/procedures of their parent study)
* Had an overall study intervention compliance ≥80% while participating in their parent study

Exclusion Criteria:

* Has discontinued study intervention in their parent study
* Has an ongoing serious adverse event considered related to study intervention by the investigator in the parent study
* Is planning to begin treatment with a nonstudy protein convertase subtilisin/kexin type 9 inhibitor (PCSK9i) while enrolled in the study
* Is currently participating in an interventional clinical study other than an enlicitide decanoate parent study

Lieu de l'étude

Institut de Cardiologie de Montreal ( Site 0504)
Institut de Cardiologie de Montreal ( Site 0504)
Montreal, Quebec
Canada

Contactez l'équipe d'étude

Primary Contact

Study Coordinator

514-376-3330
Ecogene-21 ( Site 0500)
Ecogene-21 ( Site 0500)
Chicoutimi, Quebec
Canada

Contactez l'équipe d'étude

Primary Contact

Study Coordinator

4185451252
The Medical Arts Health Research Group ( Site 0506)
The Medical Arts Health Research Group ( Site 0506)
North Vancouver, British Columbia
Canada

Contactez l'équipe d'étude

Primary Contact

Study Coordinator

250-382-4038
Diex Recherche Trois-Rivieres ( Site 0503)
Diex Recherche Trois-Rivieres ( Site 0503)
Trois-Rivieres, Quebec
Canada

Contactez l'équipe d'étude

Primary Contact

Study Coordinator

819-801-9797
North York Diagnostic and Cardiac Centre ( Site 0505)
North York Diagnostic and Cardiac Centre ( Site 0505)
North York, Ontario
Canada

Contactez l'équipe d'étude

Primary Contact

Study Coordinator

4167830000
Cambridge Cardiac Care Centre ( Site 0502)
Cambridge Cardiac Care Centre ( Site 0502)
Cambridge, Ontario
Canada

Contactez l'équipe d'étude

Primary Contact

Study Coordinator

1-888-577-8839
Étude parrainée par
Merck Sharp & Dohme LLC
Participants recherchés
Plus d'informations
ID de l'étude: NCT06492291