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Trial · NCT07442630

Long-term Comparison of Pitavastatin/Ezetimibe and Pitavastatin in Patients With Hypercholesterolemia and Elevated Triglycerides

NCT07442630, Phase 4, Active not recruiting, JW Pharmaceutical

3 sourcestrials-2026-11-12-0.5.0

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ConductScience Library. Long-term Comparison of Pitavastatin/Ezetimibe and Pitavastatin in Patients With Hypercholesterolemia and Elevated Triglycerides. Trials, record NCT07442630. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT07442630

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Trial

As registered on ClinicalTrials.gov, in the graph's capture of the registry.

Title
Long-term Comparison of Pitavastatin/Ezetimibe and Pitavastatin in Patients With Hypercholesterolemia and Elevated Triglycerides
NCT number
NCT07442630
Status
Active not recruiting
Phases
Phase 4
Enrollment
88 participants, actual
Lead sponsor
JW Pharmaceutical
Conditions
Hypercholesterolemia
Interventions
Pitavastatin 4mg, Ezetimibe 10 mg, Placebo (for Pitavastatin/Ezetimibe), Placebo (for Pitavastatin)
First posted
2026-03-02
Last updated
2026-03-02

Source ClinicalTrials.gov

Registered outcomes5

Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.

ListOutcomeTime frameDescription
PrimaryPercentage change from baseline in LDL Cholesterol at Week 8 after the first dose of study treatmentBaseline to week 8The unit of measure is percentage (%). The percentage change is calculated as: \[(Value at Week 8 - Value at Baseline) / Value at Baseline\] \* 100
SecondaryChange from baseline in HDL Cholesterol at Weeks 8, 24, and 52 after the first dose of study treatmentBaseline to week 8, 24, 52Change = (Value at Week 8, 24, or 52) - (Value at Baseline), Unit of measure: mg/dL
SecondaryChange from baseline in Triglycerides at Weeks 8, 24, and 52 after the first dose of study treatmentBaseline to week 8, 24, 52Change = (Value at Week 8, 24, or 52) - (Value at Baseline), Unit of measure: mg/dL
SecondaryChange from baseline in LDL Cholesterol at Weeks 8, 24, and 52 after the first dose of study treatmentBaseline to week 8, 24, 52Change = (Value at Week 8, 24, or 52) - (Value at Baseline), Unit of measure: mg/dL
SecondaryChange from baseline in Non-alcoholic Fatty Liver Disease Liver Fat Score (NLFS) at Weeks 24 and 52Baseline to week 24, 52The NLFS is a calculated score used to estimate liver fat content. The change is calculated as (Value at Week 24 or 52) - (Value at Baseline).

Outcomes0

Each outcome the trial posted results for, in ClinicalTrials.gov's words.

None in this release.

Results by group0

Each measurement the trial posted, group by group, in the words and numbers it posted.

None in this release.

Participant flow0

How many started, completed or left each group, period by period.

None in this release.

Adverse events0

Each adverse event the trial posted, group by group: the participants affected out of those at risk.

None in this release.

Adverse event totals0

The totals the trial posted for each group.

None in this release.

Papers0

The papers the trial lists on ClinicalTrials.gov.

None in this release.

Grants0

The grants NIH RePORTER links to the trial, newest funded first: NIH's, and some of AHRQ's, CDC's, FDA's and VA's. Each shows its title, principal investigators, organization and funder in its newest year.

None in this release.

Trial comparisons0

Comparisons of the trial's two groups, calculated by ConductScience from the counts it posted.

None in this release.

Tests0

The ConductCognition tests this trial's registered outcomes name, as ScienceGraph matched them in trial-tests-2026-11-12-0.2.1.

None in this release.

Data dates

The day each source was copied for this release.

ClinicalTrials.gov
2026-11-12
ClinicalTrials.gov
Results, from AACT
2026-03-23
AACT
NIH grant links
2026-11-13
NIH RePORTER

Sources 3

  • ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
  • ClinicalTrials.govNo license stated
  • NIH RePORTER's clinical studies and project filesPublic domain
Each source's terms
  • ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
  • ClinicalTrials.govnone stated
  • NIH RePORTER's clinical studies and project filesPublic domain (NIH RePORTER)

ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.

For software

Read this trial from software.

The record and each of its lists are JSON, twenty rows a page. No key.

GET https://conductscience.org/api/trials/v1/NCT07442630

GET https://conductscience.org/api/trials/v1/NCT07442630/registered