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Merck and Co., Inc. announced that the U.S. Food and Drug Administration has approved an expanded indication for ISENTRESS. The broadened indication now includes use in the treatment of adult patients starting HIV–1 therapy for the first time, as well as in treatment–experienced adult patients. ISENTRESS is used in combination with other antiretroviral medicines for the treatment of HIV–1 infection in adult patients. The indication for ISENTRESS is based on analyses of plasma HIV–1 RNA levels through 48 weeks in three double–blind controlled studies.

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