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A Multicenter, Open-Label Study of the Efficacy, Safety, and Pharmacokinetics of Intravenously Infused Berubicin in Adult Patients With Recurrent Glioblastoma Multiforme (WHO Grade IV) After Failure of Standard First Line Therapy

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Trial Profile

A Multicenter, Open-Label Study of the Efficacy, Safety, and Pharmacokinetics of Intravenously Infused Berubicin in Adult Patients With Recurrent Glioblastoma Multiforme (WHO Grade IV) After Failure of Standard First Line Therapy

Status: Discontinued
Phase of Trial: Phase I/II

Latest Information Update: 11 Jun 2024

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At a glance

  • Drugs Berubicin (Primary)
  • Indications Glioblastoma
  • Focus Therapeutic Use
  • Sponsors WPD Pharmaceuticals

    • Most Recent Events

    • 31 Jan 2024 Status changed from recruiting to discontinued, according to a WPD Pharmaceuticals media release.
    • 31 Jan 2024 According to a WPD Pharmaceuticals media release, company has decided to end the WPD-201 clinical trial for Berubicin in the treatment of recurrent GBM. This strategic decision comes in light of progress made by their licensor, CNS, in the potentially pivotal CNS-201 trial.
    • 26 Jan 2024 This trial has been discontinued, according to European Clinical Trials Database record.

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