跳至主要内容
临床试验/NCT00907998
NCT00907998已完成1 期

A Randomized, Double-blind, Placebo-controlled, Multiple Dose Study in Patients With Coronary Heart Disease (CHD) to Assess Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of Subcutaneous Administration of APL180

Novartis Pharmaceuticals4 个研究点 分布在 2 个国家目标入组 104 人开始时间: 2009年6月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
1 期
状态
已完成
入组人数
104
试验地点
4
主要终点
Safety and tolerability of APL180

研究概览

简要总结

The design of this study will enable an extensive evaluation of safety, tolerability, and PK-PD relationship following 4 weeks of dosing in patients with Coronary heart Disease

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Basic Science
盲法
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)

入排标准

年龄范围
18 Years 至 75 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Male and female CHD or CHD equivalent patients
  • Body mass index (BMI) must be within the range of 20 to 35 kg/m2,
  • Patient must have been on a stable statin therapy for >8 weeks prior to first dose except for the statin intolerant patients.
  • Exclusion criteria:
  • Pregnancy
  • Significant illness within two weeks prior to dosing.
  • Triglycerides ≥ 500 mg/dl (5.65 mmol/l)
  • Uncontrolled hypertension
  • Any condition that in the opinion of the investigator or the Novartis medical monitor would jeopardize the evaluation of efficacy or safety.
  • Presence of NYHA Class III or IV chronic heart failure
  • MI or angioplasty (including stenting), acute coronary syndrome (ACS), unstable angina or arterial embolic disease within 6 months prior to do Other protocol-defined inclusion/exclusion criteria may apply

排除标准

  • 未提供

研究组 & 干预措施

APL180 (first dose level)

Experimental

干预措施: APL180 (Drug)

APL180 (second dose level)

Experimental

干预措施: APL180 (Drug)

Placebo

Placebo Comparator

干预措施: Placebo (Drug)

结局指标

主要结局

Safety and tolerability of APL180

时间窗: Throughout the study

次要结局

  • Pharmacokinetics of APL180(Throughout the study)
  • Evaluate effects of APL180 biomarkers(Throughout the study)
  • Pharmacokinetic-pharmacodynamic relationship of APL180(Throughout the study)
  • Effect of APL180 on exploratory biomarkers,(Throughout the study)

研究者

申办方类型
Industry

研究点 (4)

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