← 治験一覧に戻る
心不全および慢性腎臓病患者におけるAZD9977とダパグリフロジンの有効性、安全性および忍容性
基本情報
- NCT ID
- NCT04595370
- ステータス
- 完了
- 試験のフェーズ
- 第2相
- 試験タイプ
- 介入
- 目標被験者数
- 153
- 治験依頼者名
- AstraZeneca
概要
The purpose of the study is to evaluate the efficacy and safety of AZD9977 in combination with dapagliflozin compared with dapagliflozin alone and to assess the dose-response relationship, dapagliflozin alone and 3 doses of AZD9977 combined with dapagliflozin on urinary albumin to creatinine ratio (UACR). The study will be conducted in participants with heart failure (HF) with left ventricular ejection fraction (LVEF \[below 60%\]) and chronic kidney disease (CKD) with estimated glomerular filtration rate (eGFR \[between ≥ 20 and ≤ 60 mL/min/1.73 m\^2, with at least 20% of participants with eGFR ≥ 20 to \<30 mL/min/1.73\^2 and a maximum of 35% of participants with eGFR ≥ 45 mL/min/1.73 m\^2\]).
対象疾患
Heart FailureChronic Kidney Disease
介入
AZD9977(DRUG)
Dapagliflozin(DRUG)
依頼者(Sponsor)
アストラゼネカ株式会社(INDUSTRY)