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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 Sep 12, 2026, 3:05 PM EDT

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 26, 2022
Primary completion
Mar 20, 2026
Completion
Mar 25, 2026
Last update posted
Aug 17, 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 17, 2026 · Synced Sep 12, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT05143177 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →