CN-105 in Participants with Acute Supratentorial Intracerebral Hemorrhage (CATCH) Trial.
Abstract
<h4>Background</h4>Endogenous apolipoprotein (apo) E mediates neuroinflammatory responses
and recovery after brain injury. Exogenously administered apoE-mimetic peptides effectively
penetrate the central nervous system compartment and downregulate acute inflammation.
CN-105 is a novel apoE-mimetic pentapeptide with excellent evidence of functional
and histological improvement in preclinical models of intracerebral hemorrhage (ICH).
The CN-105 in participants with Acute supraTentorial intraCerebral Hemorrhage (CATCH)
trial is a first-in-disease-state multicenter open-label trial evaluating safety and
feasability of CN-105 administration in patients with acute primary supratentorial
ICH.<h4>Methods</h4>Eligible patients were aged 30-80 years, had confirmed primary
supratentorial ICH, and were able to intiate CN-105 administration (1.0 mg/kg every
6 h for 72 h) within 12 h of symptom onset. A priori defined safety end points, including
hematoma volume, pharmacokinetics, and 30-day neurological outcomes, were analyzed.
For clinical outcomes, CATCH participants were compared 1:1 with a closely matched
contemporary ICH cohort through random selection. Hematoma volumes determined from
computed tomography images on days 0, 1, 2, and 5 and ordinal modified Rankin Scale
score at 30 days after ICH were compared.<h4>Results</h4>In 38 participants enrolled
across six study sites in the United States, adverse events occurred at an expected
rate without increase in hematoma expansion or neurological deterioration. CN-105
treatment had an odds ratio (95% confidence interval) of 2.69 (1.31-5.51) for lower
30-day modified Rankin Scale score, after adjustment for ICH score, sex, and race/ethnicity,
as compared with a matched contemporary cohort.<h4>Conclusions</h4>CN-105 administration
represents an excellent translational candidate for treatment of acute ICH because
of its safety, dosing feasibility, favorable pharmacokinetics, and possible improvement
in neurological recovery.
Type
Journal articleSubject
CATCH InvestigatorsPermalink
https://hdl.handle.net/10161/23866Published Version (Please cite this version)
10.1007/s12028-021-01287-0Publication Info
James, Michael L; Troy, Jesse; Nowacki, Nathaniel; Komisarow, Jordan; Swisher, Christa
B; Tucker, Kristi; ... CATCH Investigators (2021). CN-105 in Participants with Acute Supratentorial Intracerebral Hemorrhage (CATCH)
Trial. Neurocritical care. 10.1007/s12028-021-01287-0. Retrieved from https://hdl.handle.net/10161/23866.This is constructed from limited available data and may be imprecise. To cite this
article, please review & use the official citation provided by the journal.
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Show full item recordScholars@Duke
Michael Lucas James
Associate Professor of Anesthesiology
I have an extensive background in neuroanesthesia and neurointensive care and a special
research interest in translational and clinical research aspects of intracerebral
hemorrhage.
After completing residencies in neurology and anesthesiology with fellowships in neurocritical
care, neuroanesthesia, and vascular neurology, I developed a murine model of intracerebral
hemorrhage in the Multidisciplinary Neuroprotection Laboratories at Duke University.
After optimization of the model, I h
Jordan Komisarow
Assistant Professor of Neurosurgery
Peter George Kranz
Associate Professor of Radiology
Christopher David Lascola
Associate Professor of Radiology
Daniel Todd Laskowitz
Professor of Neurology
Our laboratory uses molecular biology, cell culture, and animal modeling techniques
to examine the CNS response to acute injury. In particular, our laboratory examines
the role of microglial activation and the endogenous CNS inflammatory response in
exacerbating secondary injury following acute brain insult. Much of the in vitro work
in this laboratory is dedicated to elucidating cellular responses to injury with the
ultimate goal of exploring new therapeutic interventions in the clinical settin
Jesse David Troy
Assistant Professor of Biostatistics & Bioinformatics
I am a biostatistician supporting research in cell therapies and regenerative medicine
at the Duke Marcus Center for Cellular Cures, and research studies in cancer therapeutics
and palliative care at the Duke Cancer Institute. I also teach biostatistics in the
Master of Biostatistics program and the <a href="
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