Safety and Efficacy of Dolutegravir in Treatment-Experienced Subjects With Raltegravir-Resistant HIV Type 1 Infection: 24-Week Results of the VIKING Study

نویسندگان

  • Joseph J. Eron
  • Bonaventura Clotet
  • Jacques Durant
  • Christine Katlama
  • Princy Kumar
  • Adriano Lazzarin
  • Isabelle Poizot-Martin
  • Gary Richmond
  • Vincent Soriano
  • Mounir Ait-Khaled
  • Tamio Fujiwara
  • Jenny Huang
  • Sherene Min
  • Cindy Vavro
  • Jane Yeo
  • Sharon L. Walmsley
  • Joseph Cox
  • Jacques Reynes
  • Philippe Morlat
  • Daniel Vittecoq
  • Jean-Michel Livrozet
  • Pompeyo Viciana Fernández
  • Jose M. Gatell
  • Edwin DeJesus
  • Jerome DeVente
  • Jacob P. Lalezari
  • Lewis H. McCurdy
  • Louis A. Sloan
  • Benjamin Young
  • Anthony LaMarca
  • Trevor Hawkins
چکیده

BACKGROUND Dolutegravir (DTG; S/GSK1349572), a human immunodeficiency virus type 1 (HIV-1) integrase inhibitor, has limited cross-resistance to raltegravir (RAL) and elvitegravir in vitro. This phase IIb study assessed the activity of DTG in HIV-1-infected subjects with genotypic evidence of RAL resistance. METHODS Subjects received DTG 50 mg once daily (cohort I) or 50 mg twice daily (cohort II) while continuing a failing regimen (without RAL) through day 10, after which the background regimen was optimized, when feasible, for cohort I, and at least 1 fully active drug was mandated for cohort II. The primary efficacy end point was the proportion of subjects on day 11 in whom the plasma HIV-1 RNA load decreased by ≥0.7 log(10) copies/mL from baseline or was <400 copies/mL. RESULTS A rapid antiviral response was observed. More subjects achieved the primary end point in cohort II (23 of 24 [96%]), compared with cohort I (21 of 27 [78%]) at day 11. At week 24, 41% and 75% of subjects had an HIV-1 RNA load of <50 copies/mL in cohorts I and II, respectively. Further integrase genotypic evolution was uncommon. Dolutegravir had a good, similar safety profile with each dosing regimen. CONCLUSION Dolutegravir 50 mg twice daily with an optimized background provided greater and more durable benefit than the once-daily regimen. These data are the first clinical demonstration of the activity of any integrase inhibitor in subjects with HIV-1 resistant to RAL.

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Dolutegravir versus placebo in subjects harbouring HIV-1 with integrase inhibitor resistance associated substitutions: 48-week results from VIKING-4, a randomized study.

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Dolutegravir in Antiretroviral-Experienced Patients With Raltegravir- and/or Elvitegravir-Resistant HIV-1: 24-Week Results of the Phase III VIKING-3 Study

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Dolutegravir – a review of the pharmacology, efficacy, and safety in the treatment of HIV

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عنوان ژورنال:

دوره 207  شماره 

صفحات  -

تاریخ انتشار 2013