New drugs on the horizon for cerebral edema: what's in the clinical development pipeline?

TitleNew drugs on the horizon for cerebral edema: what's in the clinical development pipeline?
Publication TypeJournal Article
Year of Publication2020
AuthorsRobert, SM, Reeves, BC, Alper, SL, Zhang, J, Kahle, KT
JournalExpert Opin Investig Drugs
Volume29
Issue10
Pagination1099-1105
Date Published2020 Oct
ISSN1744-7658
KeywordsAnimals, Brain Edema, Drug Development, Drug Repositioning, Drugs, Investigational, Humans, Molecular Targeted Therapy
Abstract

INTRODUCTION: Research has advanced our understanding of the molecular and cellular mechanisms of cerebral edema and has propelled the development of novel antiedema therapeutics. Current evidence supports aberrant neuro-glial ion transport as a central mechanism that underlies pathological fluid accumulation after central nervous system injury.

AREAS COVERED: Novel agents in clinical development show potential in altering the natural history and treatment of cerebral edema. Using the PubMed and Google Scholar databases, we review recent advances in our understanding of cerebral edema and describe agents under active investigation, their mechanism, and their application in recent and ongoing clinical trials.

EXPERT OPINION: Pharmacotherapies that target molecular mechanisms underlying the compensatory post-injury response of ion channels and transporters that lead to pathological alteration of osmotic gradients are the most promising therapeutic strategies. Repurposing of drugs such as glyburide that inhibit the aberrant upregulation of ion channels such as SUR1-TRPM4, and novel agents, such as ZT-1a, which reestablish physiological regulation of ion channels such as NKCC1/KCC, could be useful adjuvants to prevent and even reverse fluid accumulation in the brain parenchyma.

DOI10.1080/13543784.2020.1813715
Alternate JournalExpert Opin Investig Drugs
PubMed ID32815401
PubMed Central IDPMC8104020
Grant ListR01 NS109358 / NS / NINDS NIH HHS / United States
R01 NS111029 / NS / NINDS NIH HHS / United States
U54 HG006504 / HG / NHGRI NIH HHS / United States