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A Phase I, Open-Label, Dose-Escalation Study to Assess Safety, Tolerability and Pharmacokinetics of AZD7762 Administered as a Single Intravenous Agent and in Combination w/ Wkly Standard Dose Gemcitabine in Japanese Patients w/ Advanced Solid Malignancies.

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A Phase I, Open-Label, Dose-Escalation Study to Assess Safety, Tolerability and Pharmacokinetics of AZD7762 Administered as a Single Intravenous Agent and in Combination w/ Wkly Standard Dose Gemcitabine in Japanese Patients w/ Advanced Solid Malignancies.

Status: Discontinued
Phase of Trial: Phase I

Latest Information Update: 22 Dec 2016

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At a glance

  • Drugs AZD 7762 (Primary) ; Gemcitabine
  • Indications Solid tumours
  • Focus Adverse reactions

    • Most Recent Events

    • 04 Feb 2011 Planned End Date changed from 1 Jul 2013 to 1 Feb 2011 as reported by ClinicalTrials.gov.
    • 04 Feb 2011 Status changed from recruiting to discontinued as reported by ClinicalTrials.gov.
    • 23 Jul 2009 Status changed from not yet recruiting to recruiting as reported by ClinicalTrials.gov.

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