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Phase I accelerated dose-escalation study to determine the safety and tolerability of CYT997 when given as an oral capsule every two weeks in patients with advanced solid tumours.

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Trial Profile

Phase I accelerated dose-escalation study to determine the safety and tolerability of CYT997 when given as an oral capsule every two weeks in patients with advanced solid tumours.

Status: Completed
Phase of Trial: Phase I

Latest Information Update: 08 Jun 2016

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At a glance

  • Drugs Lexibulin (Primary)
  • Indications Solid tumours
  • Focus Adverse reactions
  • Sponsors YM BioSciences Australia

    • Most Recent Events

    • 25 Feb 2009 Status changed from recruiting to completed, as reported in the Australian New Zealand Clinical Trials Registry.
    • 26 May 2008 The expected completion date for this trial is now 1 Oct 2008.
    • 19 Dec 2007 New trial record.

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