Key result
Abelacimab prolongs clotting time across all ages in vitro, with greatest sensitivity in infants.
Why the study?
Abelacimab shows promise as a novel anticoagulant with potential reduced bleeding risk in adults and requires investigation in children.
Does abelacimab produce a concentration-dependent anticoagulant effect in pediatric plasma samples compared to adults?
Does abelacimab produce a concentration-dependent anticoagulant effect in pediatric plasma samples compared to adults?
Abelacimab demonstrates a concentration-dependent anticoagulant effect in pediatric plasma, with heightened sensitivity in infants aged 1-6 months, supporting further clinical investigation in children.
Background: Safe and effective anticoagulants are crucial for managing thrombotic disorders, particularly in children. Although direct oral anticoagulants offer advantages, including predictable pharmacokinetics and minimal monitoring, their bleeding risks remain similar to traditional anticoagulants. Abelacimab, a novel, dual-acting monoclonal antibody targeting factor XI (FXI)/activated FXI, shows promise in providing the potential for antithrombotic efficacy while reducing bleeding risks in adults and warrants further investigation in children. Objectives: testing. Methods: Citrated plasma samples from 60 healthy participants across 6 age groups (1-6 months, 6 months to 2 years, 2-6 years, 6-12 years, 12-18 years, and adults) were spiked with increasing concentrations of abelacimab (0, 0.3, 1.0, 3.0, 10, 30, and 100 μg/mL). Activated partial thromboplastin time and FXI coagulation activity were measured using commercially available reagents. Results: A sigmoidal, concentration-dependent increase in clotting time was observed across all age groups, with the 1- to 6-month age group exhibiting significantly prolonged clotting times compared with adults at most concentrations. FXI coagulation activity was comparable among all pediatric age groups and adults, with the exception of the 1- to 6-month age group. Conclusion: studies are required to confirm these findings, optimize dosing, and assess clinical implications in the pediatric population.
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Letunica et al. (2026) studied Healthy (n=60). Abelacimab vs. Adults (for age comparison) and 0 μg/mL (baseline) was evaluated on Activated partial thromboplastin time and FXI coagulation activity. In vitro spiking with abelacimab caused a concentration-dependent increase in clotting time across all ages, with significantly prolonged times in the 1- to 6-month age group compared with adults.
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