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ViiV Healthcare announces US regulatory submission for a single-tablet regimen combining dolutegravir with abacavir and lamivudine for people living with HIV
Date:10/22/2013

NCT01622790
  • ARIA (Study ING117172). A Study to Determine Safety and Efficacy of Dolutegravir/Abacavir/Lamivudine (DTG/ABC/3TC) in Human Immunodeficiency Virus (HIV)-1 Infected Antiretroviral Therapy (ART) Naive Women. National Institutes of Health Study Identifier NCT01910402.
    More information available at: http://clinicaltrials.gov/show/NCT01910402
  • Prescribing information for TIVICAY is available online at:
    https://www.viivhealthcare.com/media/58599/us_tivicay.pdfPrescribing information for EPZICOM is available online at:
    https://www.viivhealthcare.com/media/70430/us_epzicom.pdf  

     ViiV UK/U.S. Media enquiries:

    Rebecca Hunt

    +44 (0) 20 8380 6275Marc Meachem

    +1 919 483 8756GSK Global Media enquiries:

    David Daley

    +44 (0) 20 8047 5502Melinda Stubbee

    +1 919 483 2510GSK Analyst/Investor enquiries:

    Lucy Budd

    +44 (0) 20 8047 2248Tom Curry

    + 1 215 751 5419Gary Davies

    + 44 (0) 20 8047 5503James Dodwell

    + 44 (0) 20 8047 2406Jeff McLaughlin

    + 1 215 751 7002Ziba Shamsi

    + 44 (0) 20 8047 3289GlaxoSmithKline cautionary statement regarding forward-looking statements: GSK cautions investors that any forward-looking statements or projections made by GSK, including those made in this announcement, are subject to risks and uncertainties that may cause actual results to differ materially from those projected. Factors that may affect GSK's operations are described under Item 3.D "Risk factors" in the company's Annual Report on Form 20-F for 2012.


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