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临床试验/2022-501420-20-00
2022-501420-20-00招募中3 期

ISIS 678354-CS6 A Randomized, Double-Blind, Placebo-Controlled, Phase 3 Study of Olezarsen (ISIS 678354) Administered Subcutaneously to Patients with Severe Hypertriglyceridemia

Ionis Pharmaceuticals Inc.80 个研究点 分布在 11 个国家目标入组 248 人开始时间: 2023年3月28日最近更新:

试验速览

阶段
3 期
状态
招募中
入组人数
248
试验地点
80
主要终点
Percent Change from Baseline in Fasting TG Compared to Placebo [Time Frame: Baseline and Month 6]

研究概览

简要总结

To evaluate the efficacy of olezarsen as compared to placebo on the percent change in fasting triglycerides (TG) from baseline.

入排标准

年龄范围
18 years 至 65+ years(65+ Years, 18-64 Years)
接受健康志愿者

入选标准

  • Fasting TG ≥ 500 mg/dL (5.65 mmol/L) at both the Run-in period and the Qualification Period
  • Participants must be on lipid-lowering therapy that should adhere to standard of care (SOC) per local guidelines. Lipid-lowering medications should be optimized and stabilized for at least 4 weeks prior to screening to minimize changes in these medications during the study.
  • Participants must be willing to comply with diet and lifestyle

排除标准

  • Hemoglobin A1c (HbA1c) ≥ 9.5% at Screening
  • Alanine aminotransferase or aspartate aminotransferase > 3.0 × upper
  • Total bilirubin > 1.5 ULN unless due to Gilbert’s syndrome
  • Estimated GFR < 30 mL/min/1.73 m^2

结局指标

主要结局

Percent Change from Baseline in Fasting TG Compared to Placebo [Time Frame: Baseline and Month 6]

Percent Change from Baseline in Fasting TG Compared to Placebo [Time Frame: Baseline and Month 6]

次要结局

  • Percent Change from Baseline in Fasting TG Compared to Placebo [Time Frame: Baseline and Month 12]
  • Percent Change from Baseline in Fasting Apolipoprotein C-III (ApoC-III), Remnant Cholesterol and Non-High-Density Lipoprotein-Cholesterol (Non-HDL-C) Compared to Placebo [Time Frame: Baseline, Month 6 and 12]
  • Proportion of Patients who Achieve Fasting TG <500 mg/dL (5.65 mmol/L) Compared to Placebo [Time Frame: Month 12]
  • Proportion of Patients Who Achieve Fasting TG < 880 mg/dL (10 mmol/L) Compared to Placebo in the Subgroup of Patients with Baseline TG ≥ 880 mg/dL [Time Frame: Month 12]
  • Adjudicated Acute Pancreatitis Event Rate During the Treatment Period Compared to Placebo [Time Frame: Week 1 through Week 53]
  • Absolute Change in Hepatic Fat Fraction (HFF) Between Olezarsen Treatment Group and Placebo

研究者

申办方类型
Pharmaceutical company
责任方
Principal Investigator
主要研究者

Global Regulatory Affairs

Scientific

Ionis Pharmaceuticals Inc.

研究点 (80)

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