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临床试验/JPRN-jRCT2051200128
JPRN-jRCT2051200128已完成3 期

A Phase III Confirmatory Study of K-877 Extended Release Tablet-A Multicenter, Active Controlled, Randomized, Double Blind, Parallel Group Controlled Trial in Patients with dyslipidemia with high TG

Tanigawa Ryohei0 个研究点目标入组 345 人开始时间: 2021年1月29日最近更新:
适应症

试验速览

阶段
3 期
状态
已完成
发起方
入组人数
345

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
>= 20age old 至 ot applicable(—)
性别
All

入选标准

  • (1) Patients with dyslipidemia had to be age 20 years or older at written informed consent
  • (2) Patients who have received dietary or exercise guidance from 12 weeks or more prior to Screening
  • (3) Patients with the fasting serum TG >= 200 mg/dL twice consecutively at Screening

排除标准

  • (1) Patients with a fasting serum TG > 1000 mg/dL at Screening
  • (2) Patients who require administration of prohibited drugs during the clinical trial period after written informed consent
  • (3) Patients with uncontrolled thyroid disease
  • (4) Patients with type 1 diabetes and uncontrolled diabetes [HbA1c(NGSP) >= 8.0 % at Screening]
  • (5) Patients with uncontrolled hypertension (SBP >= 160 mmHg or DBP >= 100 mmHg)
  • (6) Patients with an AST or ALT three times the upper limit at Screening
  • (7) Patients with an CK five times the upper limit at Screening
  • (8) Patients with cirrhosis or those with biliary obstruction
  • (9) Patients with acute myocardial infarction within 3 months before obtaining informed consent
  • (10) Patients with heart failure class III or higher according to NYHA cardiac function classification

研究者

发起方
Tanigawa Ryohei

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