FDA Approves Botox Competitor That Lasts Longer

FRIDAY, Sept. 9, 2022 (HealthDay News) — People wanting to maintain wrinkles at bay will quickly have a brand new choice now that the US Food and Drug Administration has authorized the primary competitor for Botox in a long time.

Daxxify, made by Revance Therapeutics Inc. in Nashville, Tenn., is injected into the face alongside fear traces. It lasts longer than Botox, with about 80% of customers seeing no or delicate facial traces at 4 months after injection. For half of customers, the therapy lasted six months, the corporate mentioned in an announcement.

Users don’t have to go as soon as each three months, Dr. Balaji Prasad, who covers specialty prescription drugs as an analyst for Barclays Investment Bank, informed the New York Times. In a world the place time is of the essence, having a product with an extended length issue is extraordinarily helpful.

The new drug now enters the $3 billion discipline of facial injection medication. It can also be a neuromuscular blocking agent and a botulinum toxin, like Abbvies Botox.

It additionally opens up the door for what we will do with therapeutics, mentioned Revance CEO Mark Foley, informed the Times. If you consider migraines, cervical dystonia [a neurological condition that affects the muscles in the neck and shoulders]overactive bladder, theres an enormous medical alternative as properly.

The firm has begun testing the drug on these different medical points, Foley mentioned. While the corporate had been making an attempt to create a product that wanted no needle, it as an alternative found a method to make use of peptide know-how to maintain the product steady. Typically, animal protein or human serum is used.

Botox can also be used for extra than simply wrinkles. It has been an FDA-approved therapy for persistent migraines since 2010.

Users of Daxxify within the Revance research included some who skilled unintended effects. About 2% of individuals developed a drooping eyelid, whereas about 6% skilled headache, the corporate mentioned.

Toxin-based therapy can carry the potential for different unintended effects, resembling normal muscle weak point or respiratory difficulties, the FDA cautioned. Daxxify examine members confirmed none of these signs.

Revance had initially hoped for approval of its product in November 2020, however plans have been postponed due to pandemic journey restrictions, the Times reported. An inspection lastly performed in June 2021 discovered issues with the standard management course of and the companys working cell financial institution, which include the medication lively ingredient. Those considerations have been resolved, the Times reported.


More data

The National Library of Medicine has extra about botulinum toxin.



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