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A Safety, Tolerability and Bioavailability Study of Lisofylline After Continuous Subcutaneous (12 mg/kg) and Intravenous (9 mg/kg) Administration in Subjects With Type 1 Diabetes Mellitus

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Trial Profile

A Safety, Tolerability and Bioavailability Study of Lisofylline After Continuous Subcutaneous (12 mg/kg) and Intravenous (9 mg/kg) Administration in Subjects With Type 1 Diabetes Mellitus

Status: Recruiting
Phase of Trial: Phase I/II

Latest Information Update: 18 Sep 2021

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At a glance

  • Drugs Lisofylline (Primary) ; Lisofylline (Primary)
  • Indications Type 1 diabetes mellitus
  • Focus Adverse reactions; Biomarker

Most Recent Events

  • 18 Aug 2016 Biomarkers information updated
  • 25 May 2012 New trial record

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