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A Randomized, Double-blind, Placebo-controlled, Ascending Dose Study to Assess the Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of CNTO 5825 Following a Single Intravenous or a Single Subcutaneous Administration in Healthy Subjects.

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A Randomized, Double-blind, Placebo-controlled, Ascending Dose Study to Assess the Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of CNTO 5825 Following a Single Intravenous or a Single Subcutaneous Administration in Healthy Subjects.

Status: Completed
Phase of Trial: Phase I

Latest Information Update: 07 Oct 2010

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At a glance

  • Drugs CNTO 5825 (Primary) ; CNTO 5825 (Primary)
  • Indications Hypersensitivity
  • Focus Adverse reactions

    • Most Recent Events

    • 30 Sep 2010 Status changed from active, no longer recruiting to completed as reported by ClinicalTrials.gov.
    • 21 May 2010 Actual patient number (56) added as reported by ClinicalTrials.gov.
    • 21 May 2010 Status changed from recruiting to active, no longer recruiting as reported by ClinicalTrials.gov.

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