Study Establishes Weight-Adjusted Rivaroxaban Protocols for VTE in Children
DECEMBER 07, 2019
Guy Young, MD
The trial, which is the first to establish a dosing protocol for a liquid formulation of a direct oral anticoagulant for children 17 or under with venous thromboembolism, was presented the American Society of Hematology (ASH) 2019 annual meeting in Orlando.
“We identified the right dose for every single age group and body size from 2 kilograms to almost 140 kilograms, and all the results were within the same range of exposure and efficacy as that seen in adults,” said lead investigator and study presenter Guy Young, MD, of the Children’s Hospital Los Angeles Cancer and Blood Disease Institute and the University of Southern California Keck School of Medicine.
As part of the EINSTEIN-Jr. Program, the trial sought to establish and illustrate the dose-exposure-response relationship of rivaroxaban in children of varying size and age. Investigators had previously presented results highlighting the therapy’s safety and efficacy in children, but the ASH 2019 presentation was the first to shed light on the appropriate dosing, schedule, and formulation for administering rivaroxaban.
The trial, which was conducted between 2014-2018, included 500 children from birth to 17 years old who were randomized 2:1 to receive either rivaroxaban (n = 335) or comparator therapy (n = 165).
Investigators obtained the 24-hour area under the plasma concentration-time curve and trough and maximum steady-state plasma concentrations through population PK modeling. Additionally, exposure-response-graphs were created to assess the potential relationships of individual PK parameters with recurrent venous thromboembolism, change in thrombus burden at repeat imaging, and bleeding or adverse events.
Upon analyses, investigators found symptomatic recurrent venous thromboembolism occurred in fewer than 2% of patients treated with rivaroxaban. Investigators also noted imaging outcomes in asymptomatic children most classified as improved or normoalized—with a small percentage of patients reported no relevant change or deterioration.
When assessing the dose-exposure relationship, investigators observed the majority of individual values were within the fifth and ninety-fifth percentile for the area under the plasma concentration-time curve and trough and maximum steady-state plasma concentrations.
Investigators pointed out there was no clustering for any of the PK parameters including efficacy, bleeding, and adverse event outcomes. They concluded their child-friendly formulation observed in the trial should be applied to real-world patients, under a license which regulates rivaroxaban's use among all pediatric patients.
“This clinical trial program was meant to bring a newer, easier-to-administer, more effective, and safer medication for children—basically, a win-win-win,” Young said.
This study, titled “Rivaroxaban for Treatment of Pediatric Venous Thromboembolism: an Einstein-Jr Phase 3 Dose-Exposure-Response Evaluation,” was presented at ASH 2019.