Up to 91% of patients reached EASI-75 and up to 67% reached IGA 0/1 at week 152, with no new safety signals, according to Galderma's EADV 2026 data.
|Articles|January 6, 2009
FDA approves Allergan’s Latisse
Irvine, Calif. - The Food and Drug Administration (FDA) has approved Latisse (bimatoprost ophthalmic solution)0.03 percent for the treatment of eyelash hypotrichosis, according to Allergan.
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Irvine, Calif.
- The Food and Drug Administration (FDA) has approved Latisse (bimatoprost ophthalmic solution)0.03 percent for the treatment of eyelash hypotrichosis, according to Allergan.
Latisse will be the only FDA approved treatment to improve eyelash length, darkness and thickness, according to a press release.
Latisse will be available within the first quarter of 2009.
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