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Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of Single Rising Intravenous and Subcutaneous Doses of BI 1034020 in Healthy Male Volunteers (Partially Randomised, Single-blind, Placebo-controlled Within Dose Groups, Clinical Phase I Study)

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Trial Profile

Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of Single Rising Intravenous and Subcutaneous Doses of BI 1034020 in Healthy Male Volunteers (Partially Randomised, Single-blind, Placebo-controlled Within Dose Groups, Clinical Phase I Study)

Status: Discontinued
Phase of Trial: Phase I

Latest Information Update: 04 Aug 2015

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At a glance

  • Drugs BI 1034020 (Primary) ; BI 1034020 (Primary)
  • Indications Alzheimer's disease
  • Focus Adverse reactions
  • Sponsors Boehringer Ingelheim Pharmaceuticals

    • Most Recent Events

    • 30 May 2014 Status changed from suspended to discontinued as reported by ClinicalTrials.record.
    • 19 Mar 2014 Status changed from recruiting to suspended as reported by ClinicalTrials.gov record.
    • 30 Oct 2013 Boehringer Ingelheim has dosed the first healthy volunteers in this trial, according to an Ablynx media release. Results are expected during the second half of 2014.

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