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A Phase I, Double-blind, Randomized, Placebo Controlled, Dose Escalation Study of Valortim (MDX-1303) Administered Intravenously (IV) as a 120 Minute Infusion in Healthy, Normal Subjects.

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A Phase I, Double-blind, Randomized, Placebo Controlled, Dose Escalation Study of Valortim (MDX-1303) Administered Intravenously (IV) as a 120 Minute Infusion in Healthy, Normal Subjects.

Status: Completed
Phase of Trial: Phase I

Latest Information Update: 08 Nov 2021

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At a glance

  • Drugs MDX 1303 (Primary)
  • Indications Anthrax
  • Focus Adverse reactions

    • Most Recent Events

    • 01 Aug 2013 Status changed from active, no longer recruiting to completed, according to a PharmAthene media release.
    • 13 Apr 2011 PharmAthene completes dosing; the company anticipates safety follow-up to be completed in the third quarter of 2011 with final results available before the end of 2011.
    • 13 Apr 2011 Status changed from recruiting to active, no longer recruiting, according to a PharmAthene media release.

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