The US Food and Drug Administration (FDA) has announced its approval of Arexvy, the first respiratory syncytial virus (RSV) vaccine approved for use in the United States.
Arexvy was approved on Wednesday (May 3) for the prevention of lower respiratory tract disease caused by RSV in individuals 60 years of age and older.
The FDA granted approval of Arexvy to GlaxoSmithKline Biologicals. The application was granted Priority Review designation.
“Older adults, in particular those with underlying health conditions, such as heart or lung disease or weakened immune systems, are at high risk for severe disease caused by RSV,” said Peter Marks, MD, PhD, director of the FDA’s Center for Biologics Evaluation and Research.
The approval of the first RSV vaccine is “an important public health achievement to prevent a disease which can be life-threatening and reflects the FDA’s continued commitment to facilitating the development of safe and effective vaccines for use in the United States,” Marks added.
RSV is a highly contagious virus that causes infections of the lungs and breathing passages in individuals of all age groups. RSV circulation is seasonal, typically starting during the fall and peaking in the winter.
In older adults, RSV is a common cause of lower respiratory tract disease (LRTD), which affects the lungs and can cause life-threatening pneumonia and bronchiolitis (swelling of the small airway passages in the lungs).
According to the U.S. Centers for Disease Control and Prevention, each year in the U.S., RSV leads to approximately 60,000-120,000 hospitalizations and 6,000-10,000 deaths among adults 65 years of age and older.
The safety and effectiveness of Arexvy is based on the FDA’s analysis of data from an ongoing, randomized, placebo-controlled clinical study conducted in the U.S. and internationally in individuals 60 years of age and older.
The main clinical study of Arexvy was designed to assess the safety and effectiveness of a single dose administered to individuals 60 years of age and older. Participants will remain in the study through three RSV seasons to assess the duration of effectiveness and the safety and effectiveness of repeat vaccination.
Data for a single dose of Arexvy from the first RSV season of the study were available for the FDA’s analysis.
In the study, approximately 12,500 participants received Arexvy and 12,500 participants received a placebo.
Among the participants who received Arexvy and the participants who received a placebo, the vaccine significantly reduced the risk of developing RSV-associated LRTD by 82.6 percent and reduced the risk of developing severe RSV-associated LRTD by 94.1 percent.
Among a subset of the clinical trial participants, the most commonly reported side effects by individuals who received Arexvy were injection site pain, fatigue, muscle pain, headache and joint stiffness/pain.
Among all clinical trial participants, atrial fibrillation within 30 days of vaccination was reported in 10 participants who received Arexvy and four participants who received placebo.
In two other studies, approximately 2,500 participants 60 years of age and older received Arexvy. Some serious, albeit rare, side effects were noted.
In one of the studies in which some participants received Arexvy concomitantly with an FDA-approved influenza vaccine, two participants developed acute disseminated encephalomyelitis (ADEM), a rare type of inflammation that affects the brain and spinal cord. ADEM developed seven and 22 days respectively after receiving Arexvy and the influenza vaccine. One of the participants who developed ADEM died.
In the other study, one participant developed Guillain-Barré syndrome (a rare disorder in which the body’s immune system damages nerve cells, causing muscle weakness and sometimes paralysis) nine days after receiving Arexvy.
The FDA is requiring the company to conduct a postmarketing study to assess the signals of serious risks for Guillain-Barré syndrome and ADEM. In addition, although not an FDA requirement, the company has committed to assess atrial fibrillation in the postmarketing study.
