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临床试验/NCT01458405
NCT01458405终止1 期

Randomized, Double-Blind, Placebo-Controlled Phase I/II Study of the Safety and Efficacy of Intracoronary Delivery of Allogeneic Cardiosphere-Derived Cells in Patients With a Myocardial Infarction and Ischemic Left Ventricular Dysfunction

Capricor Inc.32 个研究点 分布在 1 个国家目标入组 135 人开始时间: 2012年11月13日最近更新:
适应症
干预措施

试验速览

阶段
1 期
状态
终止
发起方
Capricor Inc.
入组人数
135
试验地点
32
主要终点
Number of Participants Experiencing Any of the Adjudicated Events

研究概览

简要总结

The purpose of this study is to determine whether Allogeneic Cardiosphere-Derived Cells (CAP-1002) is safe and effective in decreasing infarct size in patients with a myocardial infarction.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Triple (Participant, Care Provider, Investigator)

入排标准

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

入选标准

  • 未提供

排除标准

  • 未提供

研究组 & 干预措施

Placebo

Placebo Comparator

干预措施: Placebo (Drug)

CAP-1002 Allogeneic Cardiosphere-Derived Cells

Active Comparator

干预措施: CAP-1002 Allogeneic Cardiosphere-Derived Cells (Biological)

结局指标

主要结局

Number of Participants Experiencing Any of the Adjudicated Events

时间窗: Within 1-month post-infusion

Adjudicated Events reported included: Acute myocarditis; Death due to ventricular tachycardia (VT) or ventricular fibrillation (VF); Sudden unexpected death (defined as occurring within one hour of symptom onset, or un- witnessed death); and Major adverse cardiac event (MACE) (defined as the composite incidence of death, non- fatal recurrent MI, hospitalization for heart failure, emergency room treatment for heart failure, left ventricular assist device \[LVAD\] placement or heart transplant).

Percent Change From Baseline in Myocardium Mass Infarct Size at Month 12

时间窗: Baseline, Month 12

Infarct size, expressed as a percentage, was calculated by dividing the sum of infarct areas from all sections by the sum of left ventricular (LV) areas from all sections (including those without infarct scar) and multiplying by 100. Percent improvement in infarct size defined by scar as a percent of LV mass was assessed by magnetic resonance imaging. Percent change from Baseline was calculated as: Percent change = (post-baseline value-Baseline value)/Baseline value \*100%.

次要结局

  • Absolute Change From Baseline in Left Ventricular Ejection Fraction (LVEF) at Month 6 and 12(Baseline, Month 6 and Month 12)
  • Percent Change From Baseline in Function of the Region Receiving CAP-1002 Therapy at Month 6 and 12(Baseline, Month 6 and Month 12)
  • Change From Baseline in Six-Minute Walk Test at Month 6 and 12(Baseline, Month 6 and Month 12)
  • Change From Baseline in Minnesota Living With Heart Failure Questionnaire (MLHFQ) Total Score at Month 6 and 12(Baseline, Month 6 and Month 12)
  • Number of Participants Experiencing Any of the Adjudicated Events(Up to Month 12 post-infusion)
  • Percent Change From Baseline in Left Ventricular Ejection Fraction (LVEF) at Month 6 and 12(Baseline, Month 6 and Month 12)
  • Absolute Change From Baseline in Left Ventricular End Diastolic Volume (LVEDV) at Month 6 and 12(Baseline, Month 6 and Month 12)
  • Percent Change From Baseline in Left Ventricular End Diastolic Volume (LVEDV) at Month 6 and 12(Baseline, Month 6 and Month 12)
  • Absolute Change From Baseline in Left Ventricular End Systolic Volume (LVESV) at Month 6 and 12(Baseline, Month 6 and Month 12)
  • Percent Change From Baseline in Left Ventricular End Systolic Volume (LVESV) at Month 6 and 12(Baseline, Month 6 and Month 12)
  • Absolute Change From Baseline in Infarct Size (Scar Tissue Mass) at Month 6 and 12(Baseline, Month 6 and Month 12)
  • Percent Change From Baseline in Infarct Size (Scar Tissue Mass) at Month 6 and 12(Baseline, Month 6 and Month 12)
  • Absolute Change From Baseline in Viable Mass at Month 6 and 12(Baseline, Month 6 and Month 12)
  • Percent Change From Baseline in Viable Mass at Month 6 and12(Baseline, Month 6 and Month 12)
  • Absolute Change From Baseline in Function of the Region Receiving CAP-1002 Therapy at Month 6 and 12(Baseline, Month 6 and Month 12)
  • Change From Baseline in Short Form (36) (SF-36) Scale Score at Month 6 and 12(Baseline, Month 6 and Month 12)
  • Percent Change From Baseline in Myocardium Mass Infarct Size at Month 6 and 12(Baseline, Month 6 and Month 12)
  • Change From Baseline in Log Transformed N-terminal Pro-hormone Brain Natriuretic Peptide (NT-proBNP) Biomarker at Month 6 and 12(Baseline, Month 6 and Month 12)
  • Change From Baseline in Work Productivity and Activity Impairment: Specific Health Problem (WPAI:SHP) Score at Month 6 and 12(Baseline, Month 6 and Month 12)
  • Number of Participants With Change From Baseline in Patient Global Assessment (PGA) Score at Month 6 and 12(Baseline, Month 6 and Month 12)
  • Number of Participants With Change From Baseline in New York Heart Association (NYHA) Class at Month 6 and 12(Baseline, Month 6 and Month 12)
  • Change From Baseline in N-terminal Pro-hormone Brain Natriuretic Peptide (NT-proBNP) Biomarker at Month 6 and 12(Baseline, Month 6 and Month 12)

研究者

发起方
Capricor Inc.
申办方类型
Industry
责任方
Sponsor

研究点 (32)

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