A Phase II multi-centre, randomized, open-label study investigating the pharmacokinetics, pharmacodynamics, efficacy and safety of two loading dose regimens of a new GnRH antagonist, Teverelix, long-acting formulation administered subcutaneously as three doses of 120 mg or 180 mg (given as 2 injections of 60 mg or 90 mg on Day 1, repeated on Days 2 and 3) in patients with advanced prostate cancer.

Trial Profile

A Phase II multi-centre, randomized, open-label study investigating the pharmacokinetics, pharmacodynamics, efficacy and safety of two loading dose regimens of a new GnRH antagonist, Teverelix, long-acting formulation administered subcutaneously as three doses of 120 mg or 180 mg (given as 2 injections of 60 mg or 90 mg on Day 1, repeated on Days 2 and 3) in patients with advanced prostate cancer.

Completed
Phase of Trial: Phase II

Latest Information Update: 22 Jul 2011

At a glance

  • Drugs Teverelix (Primary)
  • Indications Prostate cancer
  • Focus Therapeutic Use
  • Sponsors Ardana plc
  • Most Recent Events

    • 07 Jun 2017 Biomarkers information updated
    • 22 Jul 2011 New trial record
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