Prediction of virological response and assessment of resistance emergence to the HIV-1 attachment inhibitor BMS-626529 during 8-day monotherapy with its prodrug BMS-663068

J Acquir Immune Defic Syndr. 2013 Sep 1;64(1):7-15. doi: 10.1097/QAI.0b013e31829726f3.

Abstract

Background: BMS-663068 is the phosphonooxymethyl prodrug of BMS-626529, a small-molecule attachment inhibitor that targets the HIV-1 envelope glycoprotein gp120 preventing it from binding to CD4 T cells. In vitro investigations have demonstrated considerable variation in susceptibility of different HIV-1 isolates to BMS-626529. BMS-663068 monotherapy in HIV-1-infected subjects produced a mean maximum change from baseline of -1.64 log10 copies per milliliter, but the response was variable.

Methods: In this analysis, baseline and day 8 samples were analyzed for susceptibility to BMS-626529 and the presence of known HIV-1 attachment inhibitor resistance mutations. In addition, predictors of virological response (maximal HIV-1 RNA decline ≥1 log10 copies per milliliter) and resistance selection were investigated.

Results: The only factor associated with reduced virological response was low baseline susceptibility to BMS-626529. There was no apparent relationship between virological response and baseline treatment experience, coreceptor tropism, plasma HIV-1 RNA level, or CD4 T-cell count. Examination of all positions with known BMS-626529 resistance mutations based on in vitro selection studies showed that gp120 M426L was the primary substitution most clearly associated with nonresponse to BMS-663068. There was minimal change in susceptibility to BMS-626529 over the course of the study and no clear evidence of emergence of a known HIV-1 attachment inhibitor resistance mutation in the majority of subjects as measured by standard population-based phenotypic and genotypic approaches.

Conclusions: Nonresponse to BMS-663068 was associated with low baseline susceptibility to BMS-626529 and the presence of M426L. In this short-term trial, there was minimal evidence of selection for BMS-626529 high-level resistance over 8 days of monotherapy with BMS-663068 by population-based approaches.

Trial registration: ClinicalTrials.gov NCT01009814.

Publication types

  • Randomized Controlled Trial
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Anti-HIV Agents / pharmacology*
  • Anti-HIV Agents / therapeutic use
  • CD4 Lymphocyte Count
  • CD4-Positive T-Lymphocytes / drug effects
  • CD4-Positive T-Lymphocytes / immunology
  • Disease Susceptibility
  • Dose-Response Relationship, Drug
  • Drug Administration Schedule
  • Drug Resistance, Viral / drug effects
  • Drug Resistance, Viral / genetics
  • Female
  • HIV Envelope Protein gp120 / drug effects*
  • HIV Fusion Inhibitors / administration & dosage
  • HIV Fusion Inhibitors / pharmacology*
  • HIV Infections / drug therapy*
  • HIV Infections / genetics
  • HIV Infections / immunology
  • HIV-1 / drug effects*
  • HIV-1 / immunology
  • Humans
  • Male
  • Mutation, Missense
  • Organophosphates / therapeutic use*
  • Piperazines / therapeutic use*
  • Prodrugs / pharmacology*
  • Prodrugs / therapeutic use
  • RNA, Viral / blood
  • Treatment Outcome
  • Triazoles / therapeutic use*
  • Viral Load / drug effects*

Substances

  • Anti-HIV Agents
  • BMS-626529
  • HIV Envelope Protein gp120
  • HIV Fusion Inhibitors
  • Organophosphates
  • Piperazines
  • Prodrugs
  • RNA, Viral
  • Triazoles
  • fostemsavir

Associated data

  • ClinicalTrials.gov/NCT01009814