US FDA approves Pfizer's hair loss drug
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[June 24, 2023]
By Khushi Mandowara and Bhanvi Satija
(Reuters) - The U.S. Food and Drug Administration has approved Pfizer
Inc's drug to treat hair loss caused by an autoimmune disease, the
company said on Friday.
The drug, branded as Litfulo, has been approved for people aged 12 years
and older suffering from severe alopecia areata (AA), a condition where
the immune system attacks hair follicles and causes hair to fall out,
often in clumps.
The FDA's decision makes Litfulo the first to be allowed for the
treatment of the condition in adolescents.
The drug, which will be available in the coming weeks, is also the
second systemic treatment to gain approval after Eli Lilly's Olumiant,
used to treat the condition in adults.
"AA affects people of all ages, and not uncommonly, it affects
adolescent and younger population, so to have an approved agent for
adolescent is a significant leap forward," said Brett King, associate
professor of dermatology at Yale School of Medicine, ahead of the
decision.
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Systemic treatments usually target the cause of the disease and impact
the entire body's function including the immune system. Other treatments
for alopecia areata - which include oral steroids and topical
medications - target only certain affected parts of the body.
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A company logo is seen at a Pfizer
office in Puurs, Belgium, December 2, 2022. REUTERS/Johanna Geron/File
Photo
AA affects 300,000 people in the
U.S. each year. It gained increased attention after actor and talk
show host Jada Pinkett Smith, who suffers from the condition, was at
the center of a controversy at the Academy Awards in 2022.
Pfizer could price its product competitively with Olumiant, BMO
Capital analyst Keith Tapper said before the approval.
Olumiant has a list price of $2,622 for a 30-day supply of
2-microgram tablets or $5,244 for a 30-day supply of 4-microgram
tablets, according to Lilly's website.
Pfizer's application to the FDA was based on data from a mid- to
late-stage study that showed 80% or more hair coverage after six
months of using the drug compared to a placebo.
(Reporting by Khushi Mandowara, Bhanvi Satija and Raghav Mahobe in
Bengaluru; Editing by Sriraj Kalluvila, Devika Syamnath and Maju
Samuel)
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