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A Phase I, Dose-Escalation Study to Assess the Safety and Pharmacokinetics of SB- 485232 Administered as Five Daily Intravenous Infusions Repeated Every 28 Days in Adult Patients With Solid Tumors and Lymphomas

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Trial Profile

A Phase I, Dose-Escalation Study to Assess the Safety and Pharmacokinetics of SB- 485232 Administered as Five Daily Intravenous Infusions Repeated Every 28 Days in Adult Patients With Solid Tumors and Lymphomas

Status: Completed
Phase of Trial: Phase I

Latest Information Update: 22 Aug 2023

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At a glance

  • Drugs Iboctadekin (Primary)
  • Indications Follicular lymphoma; Solid tumours
  • Focus Adverse reactions
  • Sponsors GSK

    • Most Recent Events

    • 12 Oct 2008 Status changed from active, no longer recruiting to completed as reported by ClinicalTrials.gov.
    • 12 Sep 2005 New trial record.

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