PEANUT ALLERGY?

First-ever drug regimen could reduce life-threatening reactions.

The first-ever drug regimen to blunt acute peanut allergies in children should be approved, experts told a Food and Drug Administration committee Friday, because the therapy has the potential to reduce the risk of life-threatening reactions and improve patients’ lives.

The new drug, called Palforzia and made by Aimmune Therapeutics, is an oral immunotherapy regimen that aims to reduce sensitivity to peanut allergens. It gradually exposes children to small amounts of peanut protein over the course of six months, until they can safety eat the equivalent of two peanuts.

But the treatment does not work for everyone and is accompanied by side effects, including severe allergic reactions to the peanut exposure. Twenty percent of the children in the trial who received the treatment withdrew because of adverse events; 14% had severe allergic reactions that required treatment with epinephrine, compared with only 6.5% who received a placebo.

The regimen begins with trace amounts of the protein that are carefully measured and increased incrementally under medical supervision as tolerance develops.

The goal is not to cure the allergy but to reduce the risk that an accidental exposure to a small amount of peanut will trigger a life-threatening reaction. It might also relieve some of the fear and anxiety that some people feel about the possibility of experiencing the effects of a severe peanut allergy.

“This is one of the most important unmet needs of medicine,” said James Baker, director of the Mary H. Weiser Food Allergy Center at University of Michigan, who spoke at the advisory committee meeting on behalf of the company. He was compensated for his time.

The demand for treatment among patients and their families is enormous, Mr. Baker noted. “Right now, the only approved approach to this allergy is to avoid peanuts, and the amount of effort and cost involved in making sure everything your child is exposed to is peanut-free is overwhelming to most families,” he said.

Yet even scrupulous efforts to prevent exposures fail, resulting in life-threatening medical emergencies. “Families spend incredible efforts, often altering their entire lifestyle to practice avoidance,” Mr. Baker told the agency’s advisory committee. “The quality of life of patients and their caregivers is adversely affected due to fear and anxiety about accidental ingestions,” he added.

One in 50 American children has a peanut allergy. These allergies are believed to cause more deaths from anaphylaxis — an acute physiological response that includes lowered blood pressure, shock and constriction of the airways — than any other food allergy, though the precise number is not known.

Because children generally do not outgrow peanut allergies, they must avoid peanuts, peanut oil and foods contaminated with traces of peanuts for their entire lives.

A double-blind, placebocontrolled trial of the new drug, published last year in The New England Journal of Medicine, found that after a year, two-thirds of the 372 children who received the treatment were able to tolerate at least 600 milligrams of peanut protein — the equivalent of two peanuts — without having an allergic reaction.

Only 4% of the 124 children who had been given a placebo powder were able to consume that amount without a response.

Most of the participants were ages 4 to 17, and when they enrolled, all of them suffered from severe peanut allergies triggered by the equivalent of one-third of a peanut or less.

The trial, carried out at multiple medical centers, was designed and sponsored by Aimmune, the drug’s developer.

The drug itself consists of “defatted” peanut flour, carefully measured and packed into capsules or foil sachets of varying doses that can be easily opened and mixed with food.