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A Phase Ib, Multicentre, Double Blind, Randomized, Two-part Study, First Part Multiple Rising Dose and Second Part Two-way Cross-over, to Assess Safety, Tolerability, Efficacy and Pharmacokinetics of BI 443651 Compared to Placebo Via Respimat in Healthy Volunteers and CF Subjects.

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A Phase Ib, Multicentre, Double Blind, Randomized, Two-part Study, First Part Multiple Rising Dose and Second Part Two-way Cross-over, to Assess Safety, Tolerability, Efficacy and Pharmacokinetics of BI 443651 Compared to Placebo Via Respimat in Healthy Volunteers and CF Subjects.

Status: Completed
Phase of Trial: Phase I

Latest Information Update: 05 Nov 2021

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At a glance

  • Drugs BI 443651 (Primary)
  • Indications Cystic fibrosis
  • Focus Adverse reactions
  • Sponsors Boehringer Ingelheim

    • Most Recent Events

    • 04 Sep 2018 Status changed from active, no longer recruiting to completed.
    • 31 Jul 2018 Planned End Date changed from 18 Sep 2018 to 29 Aug 2018.
    • 31 Jul 2018 Planned primary completion date changed from 18 Sep 2018 to 29 Aug 2018.

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