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FDA approves Olumiant for treating severe alopecia areata in children 12 and older, offering new hope for hair regrowth.

Market News
25 Sep 2026
PRNewsWire
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Bullish
FDA approves Olumiant for treating severe alopecia areata in children 12 and older, offering new hope for hair regrowth.

The FDA has approved Olumiant (baricitinib), a once-daily pill, for treating severe alopecia areata (AA) in pediatric patients aged 12 and older. This approval is based on positive results from the BRAVE-AA-PEDS Phase 3 study, showing significant scalp hair regrowth and improvements in eyebrows and eyelashes after 36 weeks of treatment. Severe AA causes extensive hair loss, especially impactful during adolescence, and this new approval expands treatment options for young patients who previously had limited choices. Olumiant is already approved for adults with severe AA and rheumatoid arthritis, and this pediatric approval marks a major advancement in care for immune-mediated diseases.

Eli Lilly's recent FDA approval for Olumiant in pediatric alopecia areata patients highlights the company's ongoing innovation in health treatments. On Pluang, Eli Lilly (LLY) shares are priced at USD 1,183.55 with a slight 0.03% decrease as of Sep 26, 2026 04:21 WIB. The stock shows a market cap of $1.05 trillion and a dividend yield of 0.59%, with a typical hold time of 93 days and a balanced order activity leaning slightly towards selling at 55%.

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