FDA approves first nasal spray to treat dangerous allergic reactions (2024)

U.S. health officials on Friday approved a nasal spray to treat severe allergic reactions, the first needle-free alternative to shots like EpiPen.

The Food and Drug Administration said it approved the spray from drugmaker ARS Pharmaceuticals Inc. as an emergency treatment for adults and older children experiencing life-threatening allergic reactions known as anaphylaxis.

Anaphylaxis occurs when the body’s immune system develops a sudden, unexpected reaction to a foreign substance, such as food, insect stings or medications. Common symptoms include hives, swelling, itching, vomiting and difficulty breathing.

The device, marketed as Neffy, could upend treatment for the 33 million to 45 million Americans with severe allergies to food and other triggers. Anaphylaxis sends more than 30,000 people to emergency rooms and results in more than 2,000 hospitalizations and more than 230 deaths in the U.S. each year.

Of the 6 million prescriptions written for auto-injectors each year, more than 40% are never filled, Dr. Thomas Casale, an allergist at the University of South Florida, told an FDA advisory panel last year. Even when they are available to caregivers, many auto-injectors are used incorrectly, he said.

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“There’s a real unmet medical need for a large portion of the population,” he said.

Neffy is intended for people who weigh at least 66 pounds. It is given in a single dose sprayed into one nostril. A second dose can be given if the person’s symptoms don’t improve.

The new treatment could be life-changing for people with severe food allergies, said Dr. Kelly Cleary, a pediatrician and director with the Food Allergy Research & Education, a nonprofit advocacy group.

“I have seen the look of worry or fear,” said Cleary, whose 11-year-old son has multiple food allergies. “I worry about what happens if someone hesitates.”

Requiring an injection in an emergency is as scary to some children as the allergic reaction itself. Some parents have had to restrain thrashing children to inject them, sometimes causing cuts that require stitches. About 3,500 caregivers a year are injured when they accidentally inject themselves in the hands, ARS said.

Priscilla Hernandez, of Pasadena, California said her 12-year-old son, Zacky, who is allergic to sesame, peanuts, tree nuts, avocado and other foods, was traumatized when he had a reaction at school about six years ago and a nurse treated him with an auto-injector.

“Having to do a shot creates this whole different level of anxiety,” she said.

She said, “we are over the moon” about the FDA’s approval of the spray, which Zacky will start carrying when it becomes available.

First marketed in 1901, epinephrine predates the FDA itself. Products like the EpiPen auto-injector, approved in 1987, were authorized based on chemistry and manufacturing data and were not required to prove safety and efficacy.

Clinical trials of people experiencing potentially deadly reactions are difficult for ethical and pragmatic reasons. Instead, ARS officials compared the effect of the nasal spray on biological markers to existing epinephrine treatments.

Results showed Neffy worked about as well as injected epinephrine to boost heart rate and blood pressure, which counter severe reactions. The drug is combined with a patented agent that allows it to be easily absorbed through nasal membranes.

Other needle-free epinephrine devices are being developed to treat allergic reactions. In the pipeline are nasal sprays from Bryn Pharma, of North Carolina, and Nausus Pharma, of Israel; a needle-free auto-injector from Crossject of France; and an epinephrine film that is administered under the tongue from Aquestive Therapeutics, of New Jersey.

Neffy is designed to be easy to carry and easy to use, especially for children, said Richard Lowenthal, president and chief executive of San Diego-based ARS.

“We don’t want fear. There’s no needle, there’s no pain with this product,” he said. “It’s basically like spraying saline into your nose.”

ARS didn’t immediately disclose a list price, but said it would make the spray available through certain discount programs for about $200 per two-pack. Insurance plans must still decide whether to cover the product and at what price.

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The Associated Press Health and Science Department receives support from the Howard Hughes Medical Institute’s Science and Educational Media Group. The AP is solely responsible for all content.

FDA approves first nasal spray to treat dangerous allergic reactions (2024)

FAQs

FDA approves first nasal spray to treat dangerous allergic reactions? ›

On Aug. 9, 2024, the Food and Drug Administration (FDA) approved neffy®, an epinephrine nasal spray to treat anaphylaxis, a severe allergic reaction. It has been approved for adults and children who weigh about 66 pounds or more (30 kilograms). Neffy is a single-dose nasal spray to be given in 1 nostril.

Did FDA approve Neffy? ›

People with serious allergies now have an easier way to be helped if they begin to experience anaphylaxis. The FDA just approved “Neffy.” It's a nasal spray that has the same medication as an Epi-Pen or an Auvi-Q, but there are no needles.

What does Neffy cost? ›

Is Neffy available now? Gounder says the drug is meant to be available about eight weeks from the FDA approval. In terms of cost, the fee is about $200 out of pocket. "For people who are on commercial insurance, the cost is going to be limited to about $25," Gounder said.

How do you know if you're allergic to nasal spray? ›

Allergic reactions—skin rash, itching, hives, swelling of the face, lips, tongue, or throat. Crusting or sores in the nose. Frequent or severe nosebleeds. Low adrenal gland function—nausea, vomiting, loss of appetite, unusual weakness, fatigue, dizziness.

How does Neffy work? ›

Results showed Neffy worked about as well as injected epinephrine to boost heart rate and blood pressure, which counter severe reactions. The drug is combined with a patented agent that allows it to be easily absorbed through nasal membranes.

What has the FDA banned recently? ›

Brominated vegetable oil, sometimes listed as BVO on product labels, was recently banned from foods and beverages sold in California.

When did Auvelity get FDA approval? ›

The FDA recently approved AUVELITY, an oral medication, for the treatment of major depressive disorder in adults. August 30, 2022 - On August 19, 2022, the FDA approved AUVELITY — an oral medication manufactured by Axsome Therapeutics — for the treatment of major depressive disorder (MDD) in adults.

What is the safest nasal spray to use? ›

Over-the-counter (OTC) steroid and antihistamine nasal sprays work best to treat allergy symptoms. Flonase Allergy Relief (fluticasone), Nasacort Allergy 24 Hour (triamcinolone), and Astepro Allergy (azelastine) are common examples. They're safe for both adults and children for daily use.

Why was FLONASE taken off the market? ›

The nasal spray has been found to contain small glass particles which could block the actuator and impact the functionality of the pump. There is a potential for patients to be exposed to the glass particles and mechanical irritation cannot be ruled out.

What is the best nasal spray for seniors? ›

Steroid nasal sprays, such as Flonase (fluticasone propionate), are some of the best allergy medicines for older adults. Astepro (azelastine) nasal spray, and non-drowsy oral antihistamines, such as Allegra (fexofenadine) are also first-choice options. All of these allergy medications are safe for older adults.

What does neffy mean? ›

Neffy (epinephrine nasal) is used for the treatment of serious allergic reactions, including anaphylaxis. Neffy is used only during emergencies. Anyone using Neffy should seek medical care right away.

Am I having anaphylaxis? ›

Anaphylaxis usually begins with skin symptoms of hives or itching. Within a few minutes, you may start experiencing more severe symptoms, including: Swelling in your throat, lips and tongue. Shortness of breath.

How does Metropolol work? ›

How does metoprolol work? Metoprolol is a type of medicine called a beta blocker. Like other beta blockers, metoprolol works by changing the way your body responds to some nerve impulses, especially in the heart. It slows down your heart rate and makes it easier for your heart to pump blood around your body.

When was telithromycin approved by the FDA? ›

Approval Date: 4/01/2004.

When was Tagrisso approved by the FDA? ›

Development timeline for Tagrisso
DateArticle
Mar 31, 2017Approval Tagrisso (osimertinib) Receives FDA Full Approval
Nov 13, 2015Approval FDA Approves Tagrisso (osimertinib) for EGFR T790M Mutation-Positive Non-Small Cell Lung Cancer
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Feb 21, 2024

When is finerenone approved by the FDA? ›

Development timeline for Kerendia
DateArticle
Jul 9, 2021Approval FDA Approves Kerendia (finerenone) for the Treatment of Patients with Chronic Kidney Disease Associated with Type 2 Diabetes
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When did the FDA approve Trikafta? ›

Marketed by Vertex Pharmaceuticals, Trikafta was first approved by the FDA in 2019 for CF patients 12 and older with at least one F508del mutation, the most common mutation that causes CF. That approval has since been expanded to cover more CF-related mutations and children 6 and older.

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