A Double-Blind, Randomized, Placebo-Controlled, Single-Dose Two-Period Crossover Study to Assess the Efficacy of KAI-1678 Administered by Subcutaneous Infusion in Subjects With Spinal Cord Injury.

Trial Profile

A Double-Blind, Randomized, Placebo-Controlled, Single-Dose Two-Period Crossover Study to Assess the Efficacy of KAI-1678 Administered by Subcutaneous Infusion in Subjects With Spinal Cord Injury.

Completed
Phase of Trial: Phase II

Latest Information Update: 19 Aug 2015

At a glance

  • Drugs KAI 1678 (Primary)
  • Indications Neuropathic pain
  • Focus Therapeutic Use
  • Sponsors KAI Pharmaceuticals
  • Most Recent Events

    • 01 Jun 2010 Official title, actual number of patients (5) and lead trial centre (Trident Clinical Research), lead investigator (Bell G) added as reported by ClinicalTrials.gov.
    • 01 Jun 2010 New source identified and integrated (ClinicalTrials.gov: US National Institutes of Health record NCT01135108).
    • 01 Jun 2010 Status changed from recruiting to completed as reported by ClinicalTrials.gov.
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