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临床试验/PER-002-13
PER-002-13未知未知

A Phase 3B Study to Evaluate the Potential of Aleglitazar to Reduce Cardiovascular Risk in Patients with Stable Cardiovascular Disease and Glucose Abnormalities

F. HOFFMANN-LA ROCHE LTD.,0 个研究点目标入组 0 人开始时间: 2013年6月26日最近更新:
适应症

试验速览

阶段
未知

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
40 至 99(—)

入选标准

  • Male and female patients with established evidence of stable CVD defined as at least one of the following groups of criteria (A or B):
  • A. Age ≥ 40 years with history of a prior CV event (with onset ≥ 3 months prior to randomization and stable in the Investigator’s judgment)
  • B. Age ≥ 55 years with evidence of CVD (stable in the Investigator’s judgment), defined as at least one of the following: Coronary disease, Cerebrovascular disease or Peripheral arterial disease as defined by protocol.
  • Patients with glucose abnormalities based on one of the following A-B criteria:
  • A. Established Type 2 Diabetes mellitus (T2D) according to the 2010 ADA criteria. Treatment may include diet alone, or any approved glucose-lowering therapies except for thiazolidinediones (TZDs)
  • B. No fulfillment of criteria A but evidence of glucose abnormalities.
  • Ability and willingness to give written informed consent and to comply with the requirements of the study.
  • Optimal management of CV risk factors including hypertension and dyslipidemia as informed by the best evidence and clinical practice guidelines.

排除标准

  • Current treatment with a TZD or fibrate
  • Prior intolerance to a TZD or fibrate
  • Previous participation in a trial with aleglitazar
  • Other types of diabetes
  • Inadequate liver, hematologic or renal function as defined by protocol
  • Symptomatic congestive heart failure classified as NYHA class II-IV
  • Hospitalization for a primary diagnosis of heart failure in the 12-month period preceding the randomization
  • Peripheral edema which in the judgment of the investigator is believed to be clinically severe and of cardiac origin
  • History of surgical coronary revascularization (CABG) less than 5 years prior to screening, except in cases of subsequent myocardial infarction
  • Currently scheduled for arterial revascularization procedures
  • Systemic corticosteroid therapy for > 2 weeks, within 3 months prior to screening
  • Diagnosed or treated malignancy (except for treated cases of basal cell skin cancer, in situ carcinoma of the cervix, or in situ prostate cancer) within the past 5 years
  • Women with a positive pregnancy test, breast feeding or of childbearing potential not using medically approved, highly effective methods of contraception
  • Participation in any clinical trial.

研究者

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