Cell Repair in Heart Failure

Heart Failure Clinical Trial

Official title:

A Phase I/II, Randomised, Double-blind, Placebo Controlled, Single-centre Study of Bone Marrow Mononuclear Cells by Percutaneous Retrograde Coronary Venous Delivery to Patients With Ischaemic Heart Failure and no Standard Revascularisation Options.

Clinical Trial Details — Status: Withdrawn

Administrative data

• NCT number: NCT00285454
• Other study ID #: Amanda Heinl-Green
• Status: Withdrawn
• Phase: Phase 1/Phase 2
• First received: January 27, 2006
• Last updated: March 30, 2015
• Start date: January 2006
• Est. completion date: December 2008

Study information

• Verified date: March 2015
• Source: Imperial College London
• Contact: n/a
• Is FDA regulated: No
• Health authority: United Kingdom: Research Ethics Committee
• Study type: Interventional

Clinical Trial Summary

Many people in the UK have ischaemic heart disease. Insufficient blood supply to the heart muscle means that it functions inefficiently, and leads to symptoms of shortness of breath, chest pain and excess fluid in the body. Recently it has been shown that cells from the inside of bone are able to produce many different cell types. We are investigating a new treatment in which a patient's bone marrow cells are taken, and injected into the heart in an attempt to produce new blood vessels and heart muscle cells. This may lead to a new treatment for ischaemic heart disease.

Description:

Study Objectives:

1. Evaluate the safety of a single administration of bone marrow mononuclear cells by retrograde coronary venous delivery.

2. Evaluate the bioactivity of bone marrow mononuclear cells in mediating increased perfusion in viable underperfused areas of myocardium.

3. Evaluate the ability of bone marrow mononuclear cells to improve myocardial function specifically regional wall motion and cardiac synchronisation.

4. Evaluate the use of potential bioactivity assays and clinical outcomes for assessing bone marrow mononuclear cell- induced myocardial changes.

Study Design:

A phase I/II, randomised, double-blind, placebo controlled, single-centre study of bone marrow mononuclear cells by percutaneous retrograde coronary venous delivery to patients with ischaemic heart failure and no standard revascularisation options.

Study Population:

Patients with symptomatic ischaemic heart failure, not amenable to conventional revascularisation strategies (PCI, CABG, LVAD) or transplantation.

Independent Eligibility:

The results of the screening procedures will be compiled and submitted to an independent interventional cardiologist and cardiac surgeon who are not associated with the study for consideration for enrolment. It will be the independent reviewer's responsibility to confirm eligibility prior to a patient participating in the study.

Product:

Autologous bone marrow mononuclear, the first 6 safety and feasibility patients (open-labelled) will receive a sub-population of Indium-111 labelled cells to assess feasibility of delivery. The remaining patients will either receive Active: Bone marrow mononuclear cells and 5 % HSA Placebo: 5% HSA

Route:

Retrograde coronary venous delivery The total dose of bone marrow mononuclear cells or placebo will be divided into two, each administered as a 10ml bolus into a selective coronary veins. There will be significant patient heterogeneity regarding size of ischaemic viable territory present and anatomy of venous system. We aim to treat two veins, individual SPECT and venogram results will be used to direct the venous anatomy to be targeted. An attempt will be made to cover as large an area as possible of a patient's ischaemic viable territory. The total dose of cells will remain constant between patients.

Safety:

The first 6 patients will receive cells as an adjunct to Cardiac resynchronization Therapy and ICD. An external Data Safety and Monitoring Board has also been appointed to oversee this study.

Recruitment information / eligibility

• Status: Withdrawn
• Enrollment: 0
• Est. completion date: December 2008
• Est. primary completion date: February 2006
• Accepts healthy volunteers: No
• Gender: Both
• Age group: 18 Years to 80 Years

Eligibility

Inclusion Criteria:

1. Symptomatic ischaemic multi-vessel coronary artery disease (CAD) not suitable for standard revascularization procedures such as CABG, PCI, LVAD, or heart transplant.

2. Area of reversible inducible ischaemia (>10% of LV on SPECT) performed not more than six months prior to study treatment.

3. LVEF < 45% on optimal medical therapy.

4. NYHA class II- IV patient stable on optimal medical therapy for at least 30 days.

5. Written informed consent and agree to attend hospital appointments for 1 year.

6. Male and females 18 to 80 years of age.

Exclusion Criteria:

1. Left ventricular aneurysm or thrombus.

2. Thoracic aortic aneurysm.

3. Congenital Heart disease

4. Acute unstable angina, idiopathic cardiomyopathy, life-threatening ventricular arrhythmias, recent (less than 6 weeks).

5. Contraindication to MRI or any other study procedure.

6. Presence or history of cancer (except low grade and fully resolved non-melanoma skin malignancy).

7. Any co-morbidity likely to reduce short- term survival or which may interfere with functional testing.

8. Recent myocardial infarction < 6mths.

9. Cerebral vascular accident < 6mths.

10. Active hepatitis, receiving immunosuppressive therapy, undergoing haemodialysis.

11. Clinically significant abnormal haematology.

12. Recent history of alcoholism, drug abuse, or severe emotional, behavioural, or psychiatric problems.

13. Fertile women who are pregnant, nursing, or using no form of contraception.

14. Receiving experimental medications or participating in another study within 12 weeks of enrolment into this study.

Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double-Blind, Primary Purpose: Treatment

Related Conditions & MeSH terms

• Heart Failure
• Ischemia

Intervention

Procedure:
• Retrograde coronary venous delivery of cells.

Locations

Country	Name	City	State
United Kingdom	The Department of Gene Therapy, The National Heart and Lung Institute, Imperial College London and The Royal Brompton Hospital.	London	Middlesex

Sponsors (1)

Lead Sponsor	Collaborator
Imperial College London

Country where clinical trial is conducted

United Kingdom, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Safety: up to one year
Primary	Efficacy
Primary	Co-primary endpoints at 180 Days
Primary	Perfusion (MIBI SPECT)
Primary	Function (CMR)
Secondary	Efficacy: at 180 days
Secondary	Perfusion (CMR)
Secondary	Function (ECHO, SPECT)
Secondary	Exercise (VO2 Max)
Secondary	QOL