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Safety of LEO 43204 0.018%, 0.037% and 0.1% for Actinic Keratosis Applied Once Daily for Three Consecutive Days on Face/Chest, Scalp and Trunk/Extremities, Respectively

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Trial Profile

Safety of LEO 43204 0.018%, 0.037% and 0.1% for Actinic Keratosis Applied Once Daily for Three Consecutive Days on Face/Chest, Scalp and Trunk/Extremities, Respectively

Status: Completed
Phase of Trial: Phase II

Latest Information Update: 04 Apr 2019

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At a glance

  • Drugs Ingenol disoxate (Primary)
  • Indications Actinic keratosis
  • Focus Adverse reactions
  • Sponsors LEO Pharma

    • Most Recent Events

    • 24 Nov 2015 Status changed from recruiting to completed as reported by ClinicalTrials.gov record.
    • 10 Mar 2015 Status changed from not yet recruiting to recruiting as reported by ClinicalTrials.gov
    • 02 Feb 2015 Planned initiation date changed from 1 Jan 2015 to 1 Mar 2015 as reported by ClinicalTrials.gov

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