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A Phase I, Randomized, Open-Label, Parallel-Group, Single-Dose, Multi-Center Study in Healthy Subjects to Investigate the Bioequivalence Between a High-Concentration Formulation of Lebrikizumab Administered Subcutaneously by a Needle and Syringe and a Low-Concentration Formulation of Lebrikizumab Administered Subcutaneously by a Prefilled Syringe With Needle Safety Device (PFS-NSD)

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A Phase I, Randomized, Open-Label, Parallel-Group, Single-Dose, Multi-Center Study in Healthy Subjects to Investigate the Bioequivalence Between a High-Concentration Formulation of Lebrikizumab Administered Subcutaneously by a Needle and Syringe and a Low-Concentration Formulation of Lebrikizumab Administered Subcutaneously by a Prefilled Syringe With Needle Safety Device (PFS-NSD)

Status: Completed
Phase of Trial: Phase I

Latest Information Update: 14 Mar 2016

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At a glance

  • Drugs Lebrikizumab (Primary)
  • Indications Asthma; Atopic dermatitis; Idiopathic pulmonary fibrosis
  • Focus Pharmacokinetics
  • Sponsors Genentech

    • Most Recent Events

    • 08 Mar 2016 Status changed from active, no longer recruiting to completed as per ClinicalTrials.gov.
    • 01 Sep 2015 Status changed from recruiting to active, no longer recruiting as per ClinicalTrials.gov record.
    • 03 Jul 2015 New trial record

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