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Aimmune gets U.S. FDA approval for first peanut allergy drug


Reuters


By Carl O'Donnell

Jan 31 (Reuters) - Aimmune Therapeutics Inc said on Friday the U.S. Food and Drug Administration had approved its drug to reduce, and potentially eliminate, allergic reactions to peanuts in children aged 4 to 17 and that it had priced it at $890 per month.

The annual list price comes up to $10,680, higher than the $4,800 to $7,200 range recommended by ICER, a Boston-based independent panel that reviews drug pricing.

The treatment, called AR101 and to be sold under the brand name Palforzia, was designed to gradually reduce sensitivity to peanuts by exposing patients to a highly refined version of peanut flour over the course of several months.

The oral drug will be the in the market to offer relief from peanut allergy symptoms for those who previously had to avoid all contact with peanuts in any form or risk a reaction requiring emergency treatment with an EpiPen or another epinephrine shot

The goal, the company says, is to get allergic children and teens to the point where accidental exposure to small amounts of peanuts do not trigger a potentially life-threatening immune response.

Some 1.6 million U.S. children aged 4 to 17 live with peanut allergies, Aimmune says, creating an opportunity for peak annual sales in excess of $1 billion.

Peanut allergies are the leading cause of death from food-induced allergic reactions in the United States, with symptoms ranging from red, swollen skin to potentially deadly airway constriction.

The FDA-approved label for Palforzia includes a warning of its potential to trigger a possibly dangerous allergic response.

Aimmune said each dose increase will be done under the supervision of an allergist who is prepared to treat any allergic reactions that arise.

The list price of a drug is not necessarily what patients actually pay. Out-of-pocket costs vary based on the duration of the treatment and individual healthcare plans.

The approval comes months after an independent panel of experts to the FDA backed the allergy therapy but raised concerns about the risk of severe allergic reactions it poses to young patients.

Palforzia may soon face competition from French drugmaker DBV Technologies SA , which has filed for U.S. approval of a once-daily skin patch to reduce sensitivity to peanut exposure.

The FDA is expected to make its approval decision for DBV's Viaskin Peanut patch by August 2020.





This article appears in: Stocks , Politics
Referenced Symbols: AIMT ,



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