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Clinical Trials List

Protocol NumberD6580C00010
NCT Number(ClinicalTrials.gov Identfier)NCT04986202
Completed

2021-05-01 - 2024-09-19

Phase II/III

Not yet recruiting1

Recruiting11

Terminated1

Study ended1

ICD-10I50.20

Unspecified systolic (congestive) heart failure

ICD-10I50.21

Acute systolic (congestive) heart failure

ICD-10I50.22

Chronic systolic (congestive) heart failure

ICD-10I50.23

Acute on chronic systolic (congestive) heart failure

ICD-10I50.30

Unspecified diastolic (congestive) heart failure

ICD-10I50.31

Acute diastolic (congestive) heart failure

ICD-10I50.32

Chronic diastolic (congestive) heart failure

ICD-10I50.33

Acute on chronic diastolic (congestive) heart failure

ICD-10I50.40

Unspecified combined systolic (congestive) and diastolic (congestive) heart failure

ICD-10I50.41

Acute combined systolic (congestive) and diastolic (congestive) heart failure

ICD-10I50.42

Chronic combined systolic (congestive) and diastolic (congestive) heart failure

ICD-10I50.43

Acute on chronic combined systolic (congestive) and diastolic (congestive) heart failure

ICD-10I50.9

Heart failure, unspecified

ICD-9428.0

Congestive heart failure

A Randomised, Double-blind, Placebo-controlled, Multi-center Sequential Phase 2b and Phase 3 Study to Evaluate the Efficacy and Safety of AZD4831 Administered for Up to 48 Weeks in Participants with Heart Failure with Left Ventricular Ejection Fraction > 40%

  • Trial Applicant

  • Sponsor

    AstraZeneca

  • Trial scale

    Multi-Regional Multi-Center

  • Update

    2026/02/01

Investigators and Locations

Principal Investigator Tsung-Hsien Lin Division of Cardiovascular Diseases

Co-Principal Investigator

The Actual Total Number of Participants Enrolled

0 Recruiting

Principal Investigator I-Chang Hsieh Division of Cardiovascular Diseases

Co-Principal Investigator

  • 陳俊吉 Division of Cardiovascular Diseases
  • 謝明哲 Division of Cardiovascular Diseases

The Actual Total Number of Participants Enrolled

0 Recruiting

Principal Investigator 張瑋婷 Division of Cardiovascular Diseases

Co-Principal Investigator

The Actual Total Number of Participants Enrolled

0 Recruiting

Principal Investigator Ting-Hsing Chao Division of Cardiovascular Diseases

Co-Principal Investigator

The Actual Total Number of Participants Enrolled

0 Recruiting

Principal Investigator Kuan-Cheng Chang Division of Cardiovascular Diseases

Co-Principal Investigator

  • 盧炯睿 Division of Cardiovascular Diseases
  • 林晏年 Division of Cardiovascular Diseases
  • 吳宏彬 Division of Cardiovascular Diseases

The Actual Total Number of Participants Enrolled

0 Recruiting

Principal Investigator JIN–LONG HUANG Division of Cardiovascular Diseases

Co-Principal Investigator

  • 程遠揚 Division of Rehabilitation Medicine
  • 王奇彥 Division of Cardiovascular Diseases

The Actual Total Number of Participants Enrolled

0 Recruiting

Principal Investigator 楊甯貽 Division of Cardiovascular Diseases

Co-Principal Investigator

  • 傅鐵城 Division of Rehabilitation Medicine
  • 王美英 Division of Cardiovascular Diseases
  • 王兆弘 Division of Cardiovascular Diseases
  • 吳俐樺 Division of Cardiovascular Diseases

The Actual Total Number of Participants Enrolled

0 Recruiting

Principal Investigator Chun-Yao Huang Division of Cardiovascular Diseases

Co-Principal Investigator

The Actual Total Number of Participants Enrolled

0 Recruiting

Principal Investigator 鄭正一 Division of Cardiovascular Diseases

Co-Principal Investigator

  • 李建和 Division of Cardiovascular Diseases
  • 陳建仁 Division of Cardiovascular Diseases
  • 劉文浩 Division of Cardiovascular Diseases
  • Po-Jui Wu Division of Cardiovascular Diseases

The Actual Total Number of Participants Enrolled

0 Recruiting

Principal Investigator 郭風裕 Division of Cardiovascular Diseases

Co-Principal Investigator

  • 林克隆 Division of Rehabilitation Medicine

The Actual Total Number of Participants Enrolled

0 Recruiting

Principal Investigator Chern-En Chiang 醫研部
Taipei Veterans General Hospital

Taiwan National PI

江晨恩

Co-Principal Investigator

The Actual Total Number of Participants Enrolled

0 Recruiting

Principal Investigator 翁國昌 Division of Cardiovascular Diseases

Co-Principal Investigator

The Actual Total Number of Participants Enrolled

0 Not yet recruiting

Principal Investigator Juey-Jen Hwang Division of Cardiovascular Diseases

Co-Principal Investigator

  • 黃冠智 Division of General Internal Medicine
  • 陳文翔 Division of General Internal Medicine
  • - - Division of General Internal Medicine
  • JEN-KUANG LEE Division of General Internal Medicine
  • CHO-KAI WU Division of General Internal Medicine
  • YEN-HUNG LIN Division of General Internal Medicine
  • 莊泓叡 Division of General Internal Medicine

The Actual Total Number of Participants Enrolled

5 Study ended

Principal Investigator 劉銘恩 Division of Cardiovascular Diseases

Co-Principal Investigator

  • 陳永強 Division of Cardiovascular Diseases
  • 賴堯暉 Division of Cardiovascular Diseases
  • 林柏霖 Division of Cardiovascular Diseases
  • 吳敘平 Division of Cardiovascular Diseases
  • 劉俞旻 Division of Cardiovascular Diseases
  • 楊翔惟 Division of Cardiovascular Diseases

The Actual Total Number of Participants Enrolled

0 Terminated

Condition/Disease

Heart Failure

Objectives

Part A Primary • To evaluate the effect of AZD4831 on KCCQTSS • To evaluate the effect of AZD4831 on 6MWD

Test Drug

AZD4831

Active Ingredient

Dosage Form

Dosage

2.5mg、5mg

Endpoints

Part A
• KCCQ-TSS change from baseline at 16 weeks compared with placebo
• 6MWD change from baseline at 16 weeks compared with placebo

Inclution Criteria

1. Participant must be ≥ 40 to ≤ 85 years of age, at the time of signing the informed consent.
2. Documented stable symptomatic HF (New York Heart Association Class II-IV) for at least 1 month at Screening (Visit 1), and typical symptoms and signs of HF since at least 1 month (transient HF in the setting of an MI does not qualify) prior to Screening (Visit 1) as defined in Appendix G. Participants must be receiving an oral diuretic agent for at least 1 month prior to Visit 1 with no more than 50% dose adjustment in the last month.
3. LVEF > 40%, documented by the most recent echocardiogram, or cardiac magnetic resonance imaging within the last 12 months prior to Screening (Visit 1). All participants will undergo a local echocardiogram at the Screening (Visit 1) with central reading to confirm the LVEF > 40% eligibility criteria before randomisation.
4. 6MWD ≥ 30 meters and ≤ 400 meters at Screening (Visit 1) and Randomisation (Visit 3). Difference in 6MWD between Screening and Randomisation must be < 50 meters.

Exclusion Criteria

1. eGFR < 30 mL/min/1.73m2 by Chronic Kidney Disease-Epidemiology Collaboration formula at Screening (Visit 1).
2. Systolic blood pressure < 90 mmHg or ≥ 160 mmHg if not on treatment with ≥ 3 BP lowering medications or ≥ 180 mmHg irrespective of treatments at Randomisation (Visit 3)
3. Heart rate > 110 bpm or < 50 bpm at Randomisation (Visit 3).
4. Life expectancy < 3 years due to other reasons than cardiovascular disease.

The Estimated Number of Participants

  • Taiwan

    270 participants

  • Global

    2450 participants