US, EU Nods For Gilead's Vemlidy To Enter Saturated Hep B Market

Vemlidy, Gilead Sciences' follow-on to blockbuster hepatitis B product treatment Viread, has this week won approval in the US and been given the green light for approval in Europe – vital steps in Gilead's long term plan to protect its hep B portfolio from generic erosion.

Gilead Sciences Inc. won approval from the US FDA on Nov. 10 for its second generation hepatitis B drug Vemlidy; the compound will be priced in line with its predecessor drug, Gilead's own Viread, at $997.77 per month on the US market.

Unusually, Vemlidy also gained a positive recommendation from the European Medicines Agency's scientific committee, the CHMP, for use in hepatitis B

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