Articles

  • 1 week ago | pharma.economictimes.indiatimes.com | Deena Beasley |Julie Steenhuysen

    Los Angeles: The U.S. Food and Drug Administration on Wednesday approved Gilead Sciences lenacapavir, a twice-yearly injection, for preventing HIV infection in adults and adolescents at high risk of contracting the deadly virus. Investors and AIDS activists had been eagerly awaiting the regulatory decision for the drug seen as convenient enough to help end the 44-year-old HIV epidemic. It will be sold under the brand name Yeztugo in the U.S. at a list price of $28,218 a year.

  • 1 week ago | theglobeandmail.com | Deena Beasley |Julie Steenhuysen

  • 1 week ago | reuters.com | Deena Beasley |Julie Steenhuysen

    Gilead Sciences pharmaceutical company is seen in Oceanside, California, U.S., April 29, 2020. REUTERS/Mike Blake/File Photo June 18 (Reuters) - The U.S. Food and Drug Administration on Wednesday approved Gilead Sciences' (GILD.O), opens new tab lenacapavir, a twice-yearly injection, for preventing HIV infection in adults and adolescents. Gilead said the drug will be sold under the brand name Yeztugo. Sign up here.

  • 1 week ago | wncy.com | Julie Steenhuysen

    By Julie SteenhuysenCHICAGO (Reuters) -A U.S. government scientist who oversees the team responsible for collecting data on COVID-19 and RSV hospitalizations used to shape national vaccine policy has resigned, citing concerns over how such data would be used by the Trump administration.

  • 1 week ago | today.westlaw.com | Michael Erman |Bill Berkrot |Julie Steenhuysen

    CHICAGO (Reuters) -A U.S. government scientist who oversees the team responsible for collecting data on COVID-19 and RSV hospitalizations used to shape national vaccine policy has resigned, citing concerns over how such data would be used by the...

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