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An Open Label, Phase I Study to Evaluate the Safety, Tolerability and Pharmacokinetics of BAY94-9343 Given by Intravenous Infusion Every 3 Weeks (Q3W) in Japanese Subjects With Advanced Malignancies

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An Open Label, Phase I Study to Evaluate the Safety, Tolerability and Pharmacokinetics of BAY94-9343 Given by Intravenous Infusion Every 3 Weeks (Q3W) in Japanese Subjects With Advanced Malignancies

Status: Completed
Phase of Trial: Phase I

Latest Information Update: 06 Nov 2021

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At a glance

  • Drugs Anetumab ravtansine (Primary)
  • Indications Solid tumours
  • Focus Adverse reactions; Pharmacokinetics
  • Sponsors Bayer

    • Most Recent Events

    • 27 Jul 2017 Status changed from active, no longer recruiting to completed.
    • 07 Jun 2017 Planned End Date changed from 11 May 2018 to 31 Aug 2017.
    • 04 May 2017 Status changed from recruiting to active, no longer recruiting.

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