|Articles|August 12, 2022

FDA Approves Baloxavir Marboxil Flu Drug for Children

The FDA has approved Baloxavir Marboxil (Xofluza) for children 5 years and older to treat and prevent influenza.

This article was originally published on HCPLive.com.

The US Food and Drug Administration (FDA) has approved Genentech’s baloxavir marboxil (Xofluza) for the treatment of acute, uncomplicated influenza in healthy children aged 5 to ≤12 years old who have been symptomatic with the flu for ≤48 hours.

The supplemental New Drug Application (sNDA) for the novel antiviral therapy also indicates its use for post-exposure prevention of flu in children from the same age group who have made contact with a person infected with influenza. Baloxavir marboxil is now the first single-dose oral medication approved for treating flu in children of this age group.

This second FDA approval is based on results from the phase 3 miniSTONE-2 and BLOCKSTONE trials—the former showing baloxavir marboxil’s benefit in treating influenza in children aged 5 to ≤12 years old after 48 hours versus oseltamivir, and the latter showing its benefit as a prophylactic treatment for household members living with someone infected with influenza versus placebo.

Investigators observed common adverse events such as vomiting and diarrhea in approximately 5% of the pediatric populations treated with baloxavir marboxil in each study.

MiniSTONE-2 investigator Pedro Piedra, MD, professor of molecular virology, microbiology and pediatrics at Baylor College of Medicine, emphasized the historic and significant role of school-aged children in the community-level transmission of influenza every flu season. Per the Centers for Disease Control and Prevention (CDC), US pediatric flu cases prior to prominent public masking due to COVID-19 were upward of 6 million cases annually.

“The annual influenza vaccine continues to be the most important first step to prevent illness in children, though there can still be breakthrough cases where antiviral treatment is needed,” Piedra said in a statement. “Today’s FDA approval provides children with a single-dose antiviral option, Xofluza, to treat influenza."

Levi Garraway, MD, PhD, chief medical officer and head of Global Product Development at Genentech, praised the added indications for baloxavir marboxil to cover flu treatment and prevention of nearly every at-risk pediatric patient.

“Despite the ongoing COVID-19 pandemic, influenza continues to be a threat to public health, and effective influenza antivirals remain critical to alleviating the burden on healthcare systems,” Garraway said. “Xofluza has proven to be an important tool in fighting and preventing influenza in adults as well as adolescents, and we are pleased to now offer households and younger children our single-dose oral treatment.”


Related to this article

REMAP-CAP and the Tamiflu “Pre-Release”: A Set-Up for Disaster
Preliminary REMAP-CAP data suggesting oseltamivir may increase mortality in critically ill ICU influenza patients has sparked polarized reactions, but clinicians should await the full peer-reviewed manuscript before drawing broad conclusions, since the signal comes from a narrow, severely ill population and may reflect a therapeutic window effect rather than a blanket lack of efficacy.
GSK's mRNA Influenza Vaccine Moves to Phase 3 Trial
GSK will advance its investigational mRNA seasonal flu vaccine candidate, which targets both hemagglutinin and neuraminidase, into a phase 3 trial in September 2026 after the shot outperformed licensed flu vaccines in a phase 2 study.
Asymptomatic C difficile Colonization in Infants Doesn’t Mean Benign
A new study in infants challenges the long-standing belief about the pathogen’s effects in the youngest pediatric population. Senior author Joseph Zackular, PhD, provides insights around his work including how it reshapes gut development and offers potential intervention strategies to shield neonates.
How The Food Safety Surveillance Infrastructure Works in the US
In the first episode of our news series looking at the food safety network, Lynette Johnston, PhD, offers insights into how the federal government surveillance infrastructure operates, and how epidemiologists serve as food detectives in determining bacterial pathogens and potential foodborne outbreaks.
Ebola and the Ongoing Tale of US Failures
In mid-May, as the world was still grappling with an unexpected hantavirus outbreak aboard a tourism vessel, news broke of an Ebola outbreak in the Ituri Province of the Democratic Republic of the Congo spanning at least 3 health zones, including Bunia, Rwampara, and Mongbwalu.