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Single ascending dose study of the safety, tolerability, and pharmacokinetics of LXR-623 administered orally to healthy subjects

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Trial Profile

Single ascending dose study of the safety, tolerability, and pharmacokinetics of LXR-623 administered orally to healthy subjects

Status: Completed
Phase of Trial: Phase I

Latest Information Update: 11 Aug 2009

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At a glance

  • Drugs LXR 623 (Primary)
  • Indications Atherosclerosis
  • Focus Adverse reactions; Pharmacodynamics; Pharmacokinetics
  • Sponsors Wyeth

    • Most Recent Events

    • 22 Mar 2007 New trial record.

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