American Journal of Cardiology
Volume 95, Issue 9 , Pages 1085-1088, 1 May 2005

Effectiveness of Inhibition of Cholesteryl Ester Transfer Protein by JTT-705 in Combination With Pravastatin in Type II Dyslipidemia

  • Jan Albert Kuivenhoven, PhD

      Affiliations

    • Department of Vascular Medicine, Academic Medical Center, Amsterdam, The Netherlands
  • ,
  • Greetje J. de Grooth, MD, PhD

      Affiliations

    • Department of Vascular Medicine, Academic Medical Center, Amsterdam, The Netherlands
  • ,
  • Hitoshi Kawamura, PhD

      Affiliations

    • AKROS Pharma Inc., Princeton, New Jersey
  • ,
  • Anke H. Klerkx, PhD

      Affiliations

    • Department of Vascular Medicine, Academic Medical Center, Amsterdam, The Netherlands
  • ,
  • Francois Wilhelm, MD, PhD

      Affiliations

    • AKROS Pharma Inc., Princeton, New Jersey
  • ,
  • Mieke D. Trip, MD, PhD

      Affiliations

    • Department of Vascular Medicine, Academic Medical Center, Amsterdam, The Netherlands
  • ,
  • John J.P. Kastelein, MD, PhD

      Affiliations

    • Department of Vascular Medicine, Academic Medical Center, Amsterdam, The Netherlands
    • Corresponding Author InformationDr. Kastelein's address is: Department of Vascular Medicine, Academic Medical Center, Meibergdreef 9, Room F4-159.2, 1105 AZ Amsterdam, The Netherlands

Received 22 July 2004; accepted 16 December 2004.

The inhibition of cholesteryl ester transfer protein (CETP) has recently been shown to effectively increase high-density lipoprotein (HDL) cholesterol. This study examined the use of the CETP inhibitor JTT-705 combined with pravastatin. In a randomized, double-blind, placebo-controlled trial, 155 patients with type II dyslipidemia using pravastatin 40 mg were treated with placebo or JTT-705 300 or 600 mg. Four weeks of treatment with JTT-705 600 mg led to a 30% decrease in CETP activity (p <0.001), a 28% increase in HDL cholesterol (p <0.001), and a 5% decrease in low-density lipoprotein cholesterol (p <0.03). Combination therapy using JTT-705 and pravastatin effectively increases HDL cholesterol levels and is safe and well tolerated up to 4 weeks of administration.

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 This study was supported by a grant from AKROS Pharma Inc., Princeton, New Jersey. Dr. Klerkx was supported by a grant from the Dutch Heart Foundation, Amsterdam, The Netherlands (NHS 2000.073 and NHS 2003B191).

PII: S0002-9149(05)00189-X

doi:10.1016/j.amjcard.2004.12.064

American Journal of Cardiology
Volume 95, Issue 9 , Pages 1085-1088, 1 May 2005