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Terminated Phase 2Phase 3 Interventional

A Study to Evaluate the Efficacy and Safety of DA-1229 (Evogliptin) in Patient's Calcific Aortic Valve Disease With Mild to Moderate Aortic Stenosis (EVOID-AS)

ClinicalTrials.gov ID: NCT05143177

Public ClinicalTrials.gov record NCT05143177. 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 Nov 3, 2026, 2:07 PM EST

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

Official title

An Adaptive Phase 2/3 Multicenter, Double-Blind, Placebo-Controlled, Randomized, Parallel, 2 Arm Study to Evaluate the Efficacy and Safety of DA-1229 (Evogliptin) in Patient's Calcific Aortic Valve Disease With Mild to Moderate Aortic Stenosis (EVOID-AS)

Brief summary

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

This is an adaptive Phase 2/3 multicenter, double-blind, placebo-controlled, randomized, parallel, 2 arm study to evaluate the efficacy and safety of DA-1229 compared to placebo in patients with calcific aortic valve disease with mild to moderate aortic stenosis. There are 2 arms in this study to which patients will be randomized in a ratio of 1:1 to receive the DA-1229 or placebo orally once daily for a period of 104 weeks. The 2 arms are: placebo and DA-1229 10 mg Group. The study will have three phases: Screening Period (up to 4 weeks), Treatment Period (104 weeks), and Follow-Up Period (2-4 weeks). Total Study Duration is112 Weeks.

Study identification

NCT ID
NCT05143177
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 2, Phase 3
Lead sponsor
REDNVIA Co., Ltd.
Industry
Enrollment
486 participants

Conditions and interventions

Interventions

Drug

Eligibility (public fields only)

Age range
35 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 27, 2022 (Actual)
Primary completion
Mar 21, 2026 (Actual)
Completion
Mar 26, 2026 (Actual)
Last update posted
Aug 18, 2026

2022 – 2026

United States locations

U.S. sites
24
U.S. states
17
U.S. cities
24
Facility City State ZIP Site status
Mayo Clinic, AZ Phoenix Arizona 85054 —
University of Southern California Los Angeles California 90033 —
University of Colorado Aurora Colorado 80045 —
Mayo Clinic, FL Jacksonville Florida 32224 —
Baycare Health systems Safety Harbor Florida 34695 —
Northside Hospital Atlanta Georgia 30342 —
Massachusetts General Hospital Boston Massachusetts 02114 —
University of Michigan Ann Arbor Michigan 48109 —
Henry Ford Health System Detroit Michigan 48202 —
Beaumont Hospital, Royal Oak Royal Oak Michigan 48073 —
Mayo Clinic Rochester Minnesota 55905 —
Hackensack Meridian Health Hackensack New Jersey 07601 —
Rutgers- Robert Wood Johnson Medical School New Brunswick New Jersey 08901 —
Ichan School of Medicine New York New York 10025 —
Stony brook Stony Brook New York 11974 —
Christ Hospital Cincinnati Ohio 45219 —
OhioHealth Research Institute Columbus Ohio 43214 —
Oregon Health & Science University Portland Oregon 97239 —
University of Pittsburgh Medical Center Mechanicsburg Pennsylvania 17050 —
Einstein Medical Center Philadelphia Philadelphia Pennsylvania 19141 —
Texas Heart Institute Houston Texas 77030 —
The University of Vermont Medical Center Burlington Vermont 05401 —
Inova Health Care Services Falls Church Virginia 22042 —
Aurora Research Institute Milwaukee Wisconsin 53215 —

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

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 1 non-U.S. site.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT05143177, 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 Aug 18, 2026 · Synced Nov 3, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT05143177 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →