Ebglyss, a New Biologic Treatment for Atopic Dermatitis, Gets FDA Approval

People with moderate-to-severe atopic dermatitis, the most common form of eczema, don’t always get adequate relief from topical treatments like steroid creams and ointments. Now they have a new option: The U.S. Food and Drug Administration (FDA) just approved Ebglyss (lebrikizumab-lbkz), a biologic treatment for adults and children ages 12 years and older.

This once-a-month injectable drug belongs to a class of medicines called targeted interleukin-13 (IL-13) inhibitors, and offers a new systemic option to combat the underlying inflammation in people living with atopic dermatitis, clearing skin and alleviating itch.

The approval of Ebglyss has been highly anticipated because the data on the phase 3 studies is so strong, says Amy McMichael, MD, a dermatologist who specializes in treating people of color with dermatologic conditions at Atrium Health Wake Forest Baptist in Winston Salem, North Carolina. (Dr. McMichael was not involved in any of this research.) One study that focused exclusively on people of color determined that the medication provided consistent results no matter an individual’s skin tone.

“People can have a reduction in signs of their disease, relief from itch, and are able to reimagine what they can do with their lives now that they can function better,” says Mark Genovese, MD, senior vice president of immunology development at Eli Lilly, the drug’s manufacturer.

Nearly 40 Percent of People Achieved Clear Skin in 16 Weeks

The approval of Ebglyss is based on three pivotal phase 3 trials, ADvocate 1, ADvocate 2, and ADhere, which included a total of over 1,000 participants ages 12 and older with moderate-to-severe eczema who were unable to control their symptoms with topical prescription medications.