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A pharmacovigilance study to evaluate safety of AVODART (dutasteride) administration 0,5 mg once daily, for 52 weeks, in subjects with benign prostate hyperplasia

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Trial Profile

A pharmacovigilance study to evaluate safety of AVODART (dutasteride) administration 0,5 mg once daily, for 52 weeks, in subjects with benign prostate hyperplasia

Status: Completed
Phase of Trial: Phase IV

Latest Information Update: 22 Aug 2023

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At a glance

  • Drugs Dutasteride (Primary)
  • Indications Benign prostatic hyperplasia
  • Focus Adverse reactions
  • Sponsors GlaxoSmithKline; GSK

    • Most Recent Events

    • 05 Feb 2008 New trial record.

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