4.3 Review

Drug safety profile of integrase strand transfer inhibitors

Journal

EXPERT OPINION ON DRUG SAFETY
Volume 13, Issue 4, Pages 431-445

Publisher

TAYLOR & FRANCIS LTD
DOI: 10.1517/14740338.2014.897327

Keywords

antiretroviral therapy; dolutegravir; elvitegravir; HIV-1 infection; integrase inhibitors; integrase strand transfer inhibitors; raltegravir; safety; toxicity

Funding

  1. Fondo de Investigacion Sanitaria [08/1032, 08/1195, 09/1715, 10/2635, PI11/02512, 13/0796]
  2. Instituto de Salud Carlos III
  3. Fondos Europeos para el Desarrollo Regional (FEDER)
  4. Ministerio de Sanidad, Politica Social e Igualdad [EC11-293]
  5. Fundacion para la Investigacion y Prevencion del Sida en Espana (FIPSE ) [06/36572, 06/36610]
  6. Programa de Suport als Grups de Recerca AGAUR [2009 SGR 1061]
  7. Red de Investigacion en Sida (RIS) [RIS-EST29, RD12/0017/0001, RD12/0017/0005, RD17/0017/0022, RD17/0017/0029]
  8. Instituto de Salud Carlos III. Spain
  9. Programa de Intensificacion de Investigadores, Instituto de Salud Carlos III [INT11/240, INT12/282, INT12/383]

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Introduction: HIV-1 integrase strand transfer inhibitors (INSTIs) are a novel class of antiretroviral drugs with a good safety profile. Several INSTIs have been developed clinically. Areas covered: The purpose of this review is to examine the safety data of the three FDA-approved INSTIs: Raltegravir (RAL), Elvitegravir (EVG) and Dolutegravir (DTG). The most relevant papers related to the safety profile of integrase inhibitors were selected and summarized. Expert opinion: INSTIs have demonstrated a favorable safety profile in Phase II and III trials. The most common clinical adverse events reported were diarrhea, nausea and headache. DTG and cobicistat, a component of Stribild (TM), increase serum creatinine and decrease estimated creatinine clearance due to inhibition of active tubular secretion of creatinine without affecting renal glomerular function. INSTIs intrinsic potency, together with an outstanding safety profile, preludes an important role for these drugs to build up highly active antiretroviral treatment (HAART) in the near future.

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