Lotus Mallbris (Eli Lilly via Youtube)

Lil­ly's Olu­mi­ant gets new FDA ap­proval, nab­bing a land­mark green­light for au­toim­mune hair loss dis­ease

Pfiz­er, Con­cert Phar­ma­ceu­ti­cals and Eli Lil­ly were all gun­ning to be the first com­pa­ny to bring an alope­cia area­ta drug to mar­ket. But Lil­ly crossed the fin­ish line first Mon­day.

The In­di­anapo­lis-based phar­ma an­nounced that FDA had ap­proved JAK in­hibitor baric­i­tinib, aka Olu­mi­ant, for pa­tients with se­vere forms of the au­toim­mune dis­or­der alope­cia area­ta (AA), which re­sults in hair loss. The drug, which was ap­proved as a once-dai­ly pill in three dose lev­els of 1 mg, 2 mg and 4 mg for the in­di­ca­tion, had been orig­i­nal­ly dis­cov­ered by In­cyte be­fore Lil­ly in-li­censed it back in 2009.

Endpoints News

Unlock this article instantly by becoming a free subscriber.

You’ll get access to free articles each month, plus you can customize what newsletters get delivered to your inbox each week, including breaking news.