The Membrane-Activated Chelator Stroke Intervention (MACSI) Trial of DP-b99 in Acute Ischemic Stroke: A Randomized, Double-Blind, Placebo-Controlled, Multinational Pivotal Phase III Study

Rationale Zinc is both a direct neurotoxin and a signaling mediator in multiple early and late detrimental processes following ischemia. DP-b99, a lipophilic moderate-affinity chelator of zinc, is a first-in-class multitargeted neuroprotective agent for ischemic stroke. DP-b99 has completed several Phase I studies and two double-blind placebo-controlled Phase II trials, which supported the safety of DP-b99 and were consistent with a beneficial effect on poststroke recuperation. Aim: Membrane-Activated Chelator Stroke Intervention is a Phase III study. The primary objective is to evaluate the safety and therapeutic effects of intravenous 1·0 mg/kg/day DP-b99, initiated within nine-hours of stroke onset in patients with moderately severe hemispheric acute ischemic stroke, through the analysis across the whole distribution of scores of the primary efficacy endpoint of the modified Rankin Scale, 90 days after the stroke. Methods The Membrane-Activated Chelator Stroke Intervention study is a randomized, double-blind, placebo-controlled, multicenter, multinational, parallel-arm trial comparing a placebo group to a group treated with intravenous DP-b99 for four consecutive days. Non-rtPA-treated acute ischemic stroke patients – with a baseline NIHSS score of 10–16 and a clinical syndrome that includes language dysfunction, visual field defect and/or neglect–will be stratified on a 1:1 basis to one of the two treatments. Half will be randomized within 0–4·5 h of stroke onset. Follow-up after the four treatment days will occur on days 12, 30 and 90. An interim futility analysis will be performed after primary endpoint data have been collected for 50% of 770 subjects planned to be enrolled. A data and safety monitoring board will assess safety data and will oversee the interim analysis. Conclusion This Phase III Membrane-Activated Chelator Stroke Intervention trial is based on promising data derived from previous Phase I and II DP-b99 trials and capitalizes on lessons learned from failures of past stroke studies in relation to neuroprotection, patient selection and data analysis.

[1]  S. Neff Rodent models of stroke. , 1997 .

[2]  R. K. Hutson,et al.  Correlation of Aphasia and/or Neglect with Cortical Infarction in a Subpopulation of RANTTAS , 2001, Cerebrovascular Diseases.

[3]  M. Krakovsky,et al.  Metal ion chelation in neurodegenerative disorders , 2002 .

[4]  G. Donnan,et al.  Why lacunar syndromes are different and important. , 2004, Stroke.

[5]  J. Zivin,et al.  Neuroprotection for ischemic stroke: Two decades of success and failure , 2004 .

[6]  Alex Dmitrienko,et al.  Analysis of Clinical Trials Using SAS: A Practical Guide , 2005 .

[7]  I. Angel,et al.  Clinical pharmacology of DP-b99 in healthy volunteers: first administration to humans. , 2005, British journal of clinical pharmacology.

[8]  Bep Boode,et al.  Estimating the Number of Stroke Patients Eligible for Thrombolytic Treatment if Delay Could Be Avoided , 2006, Cerebrovascular Diseases.

[9]  H. Diener,et al.  Intravenous Thrombolysis in German Stroke Units before and after Regulatory Approval of Recombinant Tissue Plasminogen Activator , 2006, Cerebrovascular Diseases.

[10]  Alan D. Lopez,et al.  Global and regional burden of disease and risk factors, 2001: systematic analysis of population health data , 2006, The Lancet.

[11]  H. Diener,et al.  Improving Patient Selection for Clinical Acute Stroke Trials , 2006, Cerebrovascular Diseases.

[12]  M. Walters,et al.  Initial Experience of a Digital Training Resource for Modified Rankin Scale Assessment in Clinical Trials , 2007, Stroke.

[13]  M. Fisher,et al.  Future of neuroprotection for acute stroke: In the aftermath of the SAINT trials , 2007, Annals of neurology.

[14]  J. Saver Novel End Point Analytic Techniques and Interpreting Shifts Across the Entire Range of Outcome Scales in Acute Stroke Trials , 2007, Stroke.

[15]  D. Leys,et al.  Facilities Available in European Hospitals Treating Stroke Patients , 2007, Stroke.

[16]  R. Dyck,et al.  The role of zinc in cerebral ischemia. , 2007, Molecular medicine.

[17]  Scott Whyte,et al.  Perimetric homonymous visual field loss post-stroke , 2007, Journal of Clinical Neuroscience.

[18]  W. Schäbitz,et al.  A Critique of SAINT II: wishful thinking, dashed hopes, and the future of neuroprotection for acute stroke. , 2008, Stroke.

[19]  P. Sandercock,et al.  Availability of CT and MR for Assessing Patients with Acute Stroke , 2008, Cerebrovascular Diseases.

[20]  Gary A. Ford,et al.  Guidelines for management of ischaemic stroke and transient ischaemic attack 2008. , 2008, Cerebrovascular diseases.

[21]  H. Diener,et al.  DP-b99, a Membrane-Activated Metal Ion Chelator, as Neuroprotective Therapy in Ischemic Stroke , 2008, Stroke.

[22]  G. Manley,et al.  Characterizing the dose-response relationship between mannitol and intracranial pressure in traumatic brain injury patients using a high-frequency physiological data collection system. , 2008, Journal of neurotrauma.

[23]  M. Walters,et al.  Time Spent at Home Poststroke: “Home-Time” a Meaningful and Robust Outcome Measure for Stroke Trials , 2008, Stroke.

[24]  Chunxue Wang,et al.  Neuroanatomic correlation of the post-stroke aphasias studied with imaging , 2008, Neurological research.

[25]  Joseph P Broderick,et al.  National US Estimates of Recombinant Tissue Plasminogen Activator Use: ICD-9 Codes Substantially Underestimate , 2008, Stroke.

[26]  J. Torner,et al.  Baseline NIH Stroke Scale Responses Estimate the Probability of Each Particular Stroke Subtype , 2008, Cerebrovascular Diseases.

[27]  I. Sekler,et al.  The lipophilic zinc chelator DP-b99 prevents zinc induced neuronal death. , 2009, European journal of pharmacology.

[28]  V. Feigin,et al.  Worldwide stroke incidence and early case fatality reported in 56 population-based studies: a systematic review , 2009, The Lancet Neurology.

[29]  D. Mozaffarian,et al.  Heart disease and stroke statistics--2010 update: a report from the American Heart Association. , 2010, Circulation.