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U S FDA Approves CABENUVA (cabotegravir and rilpivirine) for Adolescents, Expanding the Indication of the First and Only Complete Long-Acting Injectable HIV Regimen

/PRNewswire/ The Janssen Pharmaceutical Companies of Johnson & Johnson today announced the U.S. Food and Drug Administration (FDA) has approved CABENUVA.

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U S FDA Approves Streamlined Process for Initiating HIV Therapy with CABENUVA (cabotegravir and rilpivirine), the First and Only Complete Long-Acting Injectable HIV Treatment

/PRNewswire/ The Janssen Pharmaceutical Companies of Johnson & Johnson today announced the U.S. Food and Drug Administration (FDA) has approved a label.

United statesThina abantu abashaJames mersonDanielle defeoRachael jarnaginNone of the janssen pharmaceutical companiesDrug administrationJanssen research developmentJanssen pharmaceutical companiesJanssen pharmaceutical companies of johnsonMenstar coalitionExchange commissionCompanies of johnsonJanssen sciences ireland unlimited companyDivision of janssen productsViiv healthcare

Johnson & Johnson : U S FDA Approves Streamlined Process for Initiating HIV Therapy with CABENUVA (cabotegravir and rilpivirine), the First and Only Complete Long-Acting Injectable HIV Treatment

Adults living with HIV now have an option to start injectable regimen without the need for an oral lead-in period first TITUSVILLE, N.J., March 24, 2022 - The Janssen. | March 24, 2022

United statesThina abantu abashaJames mersonDanielle defeoRachael jarnaginNone of the janssen pharmaceutical companiesDrug administrationJanssen research developmentJanssen pharmaceutical companiesJanssen pharmaceutical companies of johnsonMenstar coalitionExchange commissionCompanies of johnsonJanssen sciences ireland unlimited companyDivision of janssen productsViiv healthcare

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