Year: 2026
Type: article
Abstract: Targeting the contact activation system through Factor XI (FXI) or Factor XII (FXII) inhibition represents a major paradigm shift in antithrombotic therapy for ischemic stroke. Unlike traditional anticoagulants, contact pathway factors drive pathological thrombus propagation and thromboinflammation; crucially, while FXII plays a negligible role in physiological hemostasis, FXI contributes only secondarily, thereby substantially uncoupling antithrombotic efficacy from major bleeding risk. However, a notable disconnect exists between experimental models and clinical development. Preclinical stroke literature, primarily rodent middle cerebral artery occlusion (MCAO) models, is overwhelmingly concentrated on FXII targeting, where FXII deficiency or blockade consistently reduces cerebral infarct volumes, preserves microvascular perfusion, and attenuates thromboinflammation, whereas experimental studies of direct FXI treatment remain sparse. Conversely, human clinical translation has focused largely on oral FXIa inhibitors, maintaining a favorable bleeding profile across indications but yielding mixed efficacy, ranging from neutral Phase II studies and the early termination of OCEANIC-AF to positive secondary stroke prevention data. Following positive OCEANIC-STROKE findings, asundexian (under FDA priority review as of September 2026) emerges as a prospective add-on to antiplatelet therapy for the secondary prevention of noncardioembolic stroke or high-risk TIA, particularly in nonlacunar or atherosclerotic populations. Reconciling preclinical FXII data with clinical FXIa trial outcomes provides a timely rationale to systematically review evidence across MCAO models and human stroke trials to delineate the distinct therapeutic potentials of FXI and FXII inhibition.
Institution: Essen University Hospital
Language: English
Subfield: Genetics
Field: Medicine
Domain: Health Sciences
Open Access status: gold
Estimated APC paid: $2,190
OpenAlex ID: W7222567147