CHEER Trial Switch from Enfuvirtide to Raltegravir CHEER: Study - - PowerPoint PPT Presentation

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CHEER Trial Switch from Enfuvirtide to Raltegravir CHEER: Study - - PowerPoint PPT Presentation

Switch from Enfuvirtide to Raltegravir CHEER Trial Switch from Enfuvirtide to Raltegravir CHEER: Study Design Study Design: CHEER Background : Prospective, nonrandomized, open-label, historical control study evaluating switch from


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SLIDE 1

Switch from Enfuvirtide to Raltegravir

CHEER Trial

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SLIDE 2

Switch from Enfuvirtide to Raltegravir

CHEER: Study Design

Source: Towner W, et al. J Acquir Immune Defic Syndr. 2009;51:367-73.

Raltegravir 400 mg BID + background ART

(n = 52)

Study Design: CHEER

  • Background: Prospective, nonrandomized,
  • pen-label, historical control study evaluating

switch from enfuvirtide to raltegravir in virologically suppressed adults with HIV.

  • Inclusion Criteria (n =52)
  • Age ≥18 years
  • HIV RNA <50 copies/mL (by PCR) or

<75 copies/mL (by bDNA) for ≥6 months

  • No prior treatment with integrase inhibitors
  • Treatment Arm
  • Raltegravir + background antiretroviral regimen

(patients served as own controls)

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SLIDE 3

Switch from Enfuvirtide to Raltegravir

CHEER: Results

Week 24: Virologic Response (Non-completer=Failure, ITT Analysis)

Source: Towner W, et al. J Acquir Immune Defic Syndr. 2009;51:367-73.

94 20 40 60 80 100 Virologic Suppression (%)

Post-switch to Raltegravir

49/52

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SLIDE 4

Switch from Enfuvirtide to Raltegravir

CHEER: Conclusions

Source: Towner W, et al. J Acquir Immune Defic Syndr. 2009;51:367-73.

Conclusions: “In treatment-experienced patients on a stable virologically suppressive enfuvirtide-containing regimen, raltegravir can safely be substituted for enfuvirtide.”

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SLIDE 5

Acknowledgment

The National HIV Curriculum is an AIDS Education and Training Center (AETC) Program supported by the Health Resources and Services Administration (HRSA) of the U.S. Department of Health and Human Services (HHS) as part of an award totaling $800,000 with 0% financed with non-governmental sources. This project is led by the University of Washington’s Infectious Diseases Education and Assessment (IDEA) Program.

The content in this presentation are those of the author(s) and do not necessarily represent the official views of, nor an endorsement, by HRSA, HHS, or the U.S. Government.