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Completed Phase 2 Interventional Results available

Study to Investigate the Efficacy and Pharmacokinetic Profile of K-877-ER Compared to K-877-IR

ClinicalTrials.gov ID: NCT04447820

Public ClinicalTrials.gov record NCT04447820. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 17, 2026, 11:53 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Multicenter, Randomized, Open-Label, 4-Week Study to Investigate the Efficacy and Pharmacokinetic Profile of K-877-ER Once Daily Treatment Compared to K-877-IR Twice Daily Treatment in Adult Patients With Fasting Triglyceride Levels

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

A study to evaluate the efficacy of K-877 extended release (ER) once daily (QD) compared to K-877 immediate release (IR) twice daily (BID).

Study identification

NCT ID
NCT04447820
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Kowa Research Institute, Inc.
Industry
Enrollment
96 participants

Conditions and interventions

Conditions

Interventions

Drug

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Jun 10, 2020 (Actual)
Primary completion
Dec 3, 2020 (Actual)
Completion
Dec 3, 2020 (Actual)
Last update posted
Dec 22, 2023

2020

United States locations

U.S. sites
12
U.S. states
9
U.S. cities
12
Facility City State ZIP Site status
Pinnacle Research Group Anniston Alabama 36207 —
Jacksonville Center for Clinical Research Jacksonville Florida 32216 —
Progressive Medical Research Port Orange Florida 32127 —
Columbus Regional Health Columbus Georgia 31904 —
Prism Research Saint Paul Minnesota 55114 —
Diabetes and Endocrinology Consultants, P.C. Morehead City North Carolina 28557 —
Medpace Clinical Pharmacology, LLC Cincinnati Ohio 45227 —
Aventiv Research, Inc. Columbus Ohio 43213 —
Summit Research Group, LLC Munroe Falls Ohio 44262 —
Health Concepts Rapid City South Dakota 57702 —
Clinical Trials of Texas, Inc. San Antonio Texas 78229 —
Manassas Clinical Research Center Manassas Virginia 20110 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT04447820, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Dec 22, 2023 · Synced Oct 17, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT04447820 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →