Recent months have seen the approval or advancement of studies on various nasal sprays to treat or prevent common conditions, based on clinical trials that demonstrated the efficacy of this way of administering medicine, far removed from traumatic needle sticks or the need to swallow pills.
The US Food and Drug Administration (FDA) just approved Neffy, the first epinephrine nasal spray to treat allergic reactions (type I), including those that are life‑threatening (anaphylaxis).
This nasal spray can be used in adult and pediatric patients who weigh at least 30 kg (about 66 pounds).
Allergic reactions occur when a person’s immune system reacts abnormally to a substance that does not normally cause symptoms. Anaphylaxis is a serious, life‑threatening allergic reaction that typically affects multiple parts of the body and is considered a medical emergency.
Common allergens that can induce anaphylaxis include certain foods, medications, and insect stings. Symptoms typically appear within minutes of exposure and include urticaria (hives), swelling, itching, vomiting, difficulty breathing, and loss of consciousness, among others.
Epinephrine is the only life‑saving treatment for anaphylaxis and, until now, it had only been available for patients as an injection.
Neffy is a single‑dose nasal spray that is administered into a nostril. Just like injectable epinephrine products, a second dose (using a new nasal spray to administer Neffy into the same nostril) may be administered if there is no improvement of symptoms or if symptoms worsen.
There are more than 1,100 trials involving nasal sprays on the website
clinicaltrials.gov, which hosts information on most ongoing or past clinical studies in the United States and the world.
Experts believe that sprays are becoming more widely used to administer medication because they can “bypass” the first step of metabolism in the liver, allowing the drug to enter the circulatory system directly. This is an advantage when
quick absorption of the medication and rapid onset of action are desired. They also reduce the side effects that can occur with systemic drug administration.
Because they are
self‑administered, it is important that health professionals explain the
correct way to use sprays to their patients.
Some of the most recent new medicines available as nasal sprays include:
Allergy sufferers bore witness to a historic moment on March 15, 2024, when the
FDA approved the nasal spray fluticasone propionate (XHANCE) for the treatment of chronic rhinosinusitis without nasal polyps in adult patients. It is the first and only drug to have received this indication in the agency’s history. Approval was based on data from the phase 3 ReOpen program and came just over a year after Optinose announced that it was submitting its new drug to the FDA.
A large study published in
The Lancet Respiratory Medicine looked at the benefit of accessible, simple interventions used preventatively or early in respiratory illness in primary care settings. When used at the first sign of respiratory infection, two nasal sprays were shown to have a clinically significant effect on the duration of illness compared to usual care. They also reduced the number of workdays lost and, when used with two other interventions, the use of antibiotics.
Researchers from the University of Texas Medical Branch recently made a significant discovery in the fight against neurodegenerative illnesses like Alzheimer’s and dementia. The study, published in
Science Translational Medicine, presented an innovative nasal spray treatment that yielded promising results in clearing harmful tau protein aggregates and improving cognitive function in models of aged mice with neurodegenerative diseases. Current tau immunotherapies have struggled to be effective due to their limited ability to penetrate the intracellular compartments where these tau aggregates reside and which, when damaged, accelerate Alzheimer’s disease.