CTIS2023-509192-16-00进行中(未招募)1 期
A study to Assess the Effect of Vonafexor on Kidney Function in Subjects With Impaired Renal Function and Suspected MASH - EYP001-210
适应症
试验速览
- 阶段
- 1 期
- 状态
- 进行中(未招募)
- 发起方
- ENYO Pharma
- 入组人数
- 50
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
入排标准
- 年龄范围
- 18 至 65+(—)
- 性别
- All
入选标准
- •Male or female subject., Age between 18 and 75 years, both inclusive., Overweight or obesity (body mass index BMI = 25.0 kg/m2 and = 45.0 kg/m2) with or without type 2 diabetes mellitus (T2DM with an HbA1c = 9.5%)., eGFR = 30 and < 90 (mL/min/1.73 m²)., Presumed mild to higher liver fibrosis as shown by a FIBROTEST score = 0.28 and/or FIB-4 score = 1.3.
排除标准
- •Known or suspected hypersensitivity to IMP or any of the excipients or to any component of the IMP formulation., History of multiple and/or severe allergies to drugs including contrast media or foods or a history of severe anaphylactic reaction., Known non-MASH liver disease., History or presence of cirrhosis., Proteinuria in the nephrotic range with a protein-to-creatinine ratio > 3.5 g protein/g creatinine (350 mg/mmol).
研究者
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