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CompletedNCT02748057

A Clinical Trial to Assess the Long Term Safety and Tolerability of MK-0653H in Japanese Participants With Hypercholesterolemia (MK-0653H-833)

A Phase III, Open-label, Clinical Trial to Assess the Long Term Safety and Tolerability of MK-0653H in Japanese Patients With Hypercholesterolemia Who Have Inadequate LDL-C Control on Ezetimibe or Rosuvastatin Monotherapy

Status
Completed
Phase
Phase 3
Study type
Interventional
Enrollment
135 (actual)
Sponsor
Organon and Co · Industry
Sex
All
Age
20 Years – 80 Years
Healthy volunteers
Not accepted

Summary

The study will assess the safety and tolerability of Ezetimibe 10 mg+ Rosuvastatin 2.5 mg and Ezetimibe 10 mg+ Rosuvastatin 5.0 mg for up to 52 weeks in Japanese participants with hypercholesterolemia uncontrolled with monotherapy of Ezetimibe 10 mg or Rosuvastatin up to 5 mg.

Conditions

Interventions

TypeNameDescription
DRUGEzetimibe
DRUGRosuvastatin

Timeline

Start date
2016-05-18
Primary completion
2017-12-11
Completion
2017-12-11
First posted
2016-04-22
Last updated
2024-05-16
Results posted
2018-12-04

Source: ClinicalTrials.gov record NCT02748057. Inclusion in this directory is not an endorsement.

A Clinical Trial to Assess the Long Term Safety and Tolerability of MK-0653H in Japanese Participants With Hypercholeste (NCT02748057) · Clinical Trials Directory