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临床试验/ACTRN12615001144505
ACTRN12615001144505终止1 期

A Phase I/IIa Study investigating the safety and tolerability of intramuscular DVC1-0101 compared with placebo in patients with Intermittent Claudication or Critical Limb Ischaemia Secondary to Peripheral Artery Disease.

CMAX - a division of IDT Australia0 个研究点目标入组 3 人开始时间: 2015年10月28日最近更新:

试验速览

阶段
1 期
状态
终止
发起方
入组人数
3

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional
分配方式
Randomised controlled trial
主要目的
Treatment
盲法
Blinded (masking used)

入排标准

年龄范围
40 Years 至 o limit(—)
性别
All

入选标准

  • Diagnosis of PAD secondary to atherosclerosis, confirmed by medical history and one of the following observed in either leg at the screening visit:
  • a.Resting ABI less than or equal to 0.90
  • b.Resting ABI greater than 0.90 and less than or equal to 1.30, with a reduction of greater than or equal to 0.20 in ABI when measured within 2 minutes after completion of treadmill exercise.
  • c.TBI less than 0.75 if the subject has non-compressible calf arteries. i.e. Rutherford category 1-5. (Rutherford RJ, 1997)
  • Claudication symptoms of stable severity for at least 3 months prior to screening OR the highest ACD from either the screening or baseline exercise treadmill test (ETT), utilizing a modified Gardner protocol, must be between 1 and 12 minutes (inclusive).

排除标准

  • PAD secondary to non-atherosclerotic conditions.
  • Proximal severe obstructive disease amenable to revascularisation.
  • Lower extremity amputation(s), including a toe amputation, which interfere(s) with walking on the treadmill.
  • Percutaneous revascularization procedure within 3 months prior to Screening, or procedures that are planned during the study.
  • Poorly controlled diabetes mellitus as evidenced by a haemoglobin A1C (HbA1c) > 12%.
  • Coronary artery bypass graft surgery (CABG), open peripheral vascular revascularization, or major surgical procedures within 3 months prior to screening, or planned at any time during the study
  • Unstable cardiovascular disease (CVD), defined as unstable both by clinical criteria and / or major changes in medication within 3 months prior to Screening or Baseline of the Extension Period.
  • History of congestive heart failure (CHF) or presence of CHF as defined by modified Framingham criteria class II- IV.
  • Myocardial infarction (MI) within 3 months prior to Screening or at Baseline of the Extension Period.

研究者

发起方
CMAX - a division of IDT Australia

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