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Published byBelinda Gregory Modified over 9 years ago
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4th International Symposium on Stem Cell Therapy Madrid, April 26-27, 2007 Stem Cell Thertapy for STEMI. Is is Time for a Large Scale Clinical Trial ? Contra
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Cardiac Cell Therapy Lessons Fom Early Trials - Heterogeneity of patient populations and outcome measurements - Usual lack of full characterization of the final cell therapy product - Diversity of dosing protocols, application schedules and routes of cell delivery
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Time for a Large Scale Clinical Trial ?
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Skeletal Myoblasts - Isolation of precursors of cardiomyocytes - Prevention of arrhythmias by connexin-43 engineering - Identification of an immature subpopulation featuring a low antigenicity Time for a Large Scale Clinical Trial ?
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Bone Marrow-Derived Cells - Cell type (MNC, CD34 + /CD133 + progenitors, MSC) - Dose ranging - Enhancement of myocardial homing Time for a Large Scale Clinical Trial ?
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AutologousAllo/Xenogeneic Availability +++ +++ Reproductibility - +++ Immunogenicity - ++/+++ Cost +++ + Autologous vs. Allo/Xenogeneic Cell Therapy Products : A Difficult Trade-Off
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Cell Therapy : EMEA Guidelines Objectives of Preclinical Development - To demonstrate proof-of-principle - To provide information allowing : to select safe doses for clinical trials to support the route of administration, duration of exposure and application schedule to indicate the duration of follow-up time for detecting adverse reactions - To identify target organs for toxicity and parameters to monitor in patients
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Cell Therapy : EMEA Guidelines Quality & Manufacturing Aspects - Traceability of starting and raw materials - Manufacturing process ensuring product consistency - Characterization of the final product in terms of identity (phenotypic and genotypic profiles), purity, potency, viability & tumourigenicity - Quality controls (release criteria, stability testing) - Validation of the manufacturing process
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The MAGIC Trial : Preliminary Lessons Difficulties of Surgical Trials - Declining referrals for CABG - Restricted space for additional improvements - Background noise due to heterogeneity in practice patterns
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Stanley K, Circulation 2007;115:1819-22. Characteristics of a High-Quality RCT
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J Thorac Cardiovasc Surg 2006;132:243-4 Begg et al. JAMA 1996;276:637-9.
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Adapted from the Coronary Drug Project Research Group, New Engl J Med 1980;303:1038-41 Importance of Placebo Groups
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Adapted from the Coronary Drug Project Research Group, New Engl J Med 1980;303:1038-41 Importance of Placebo Groups
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Tiruvoipati et al. J Thorac Cardiovasc Surg 2006;132:233-40. Awareness of the CONSORT Statement and Views of Authors Reporting RCTs in Major Cardiothoracic Journals
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Randomized Multicentre Trials Errors in Trial Design & Assessment - Inappropriate control groups - Inadequate sizing of study groups - Lack of blinding during outcome assessment - Uncautious use of composite end points - Failure to correct for repeated data analysis during the trial - Excessive reliance on = 0.05 and lack of correction for multiple comparisons
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