The FDA expanded the label for Gilead’s hepatitis B drug Vemlidy on Thursday to patients as young as 6 years old.
Vemlidy, or tenofovir alafenamide, is a once-daily treatment for chronic hepatitis B that pulled in $862 million in sales for Gilead in 2023, up from $842 million in 2022.
The regulator originally approved the therapy in 2016 for adults with chronic hepatitis B infections and compensated liver disease. Then in 2022, the label was expanded to include patients who are at least 12 years old with the infection and compensated liver disease.
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