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A PHASE 1, RANDOMIZED, DOUBLE-BLIND, THIRD-PARTY OPEN, PLACEBO-CONTROLLED, DOSE ESCALATING STUDY TO EVALUATE THE SAFETY, TOLERABILITY, PHARMACOKINETICS AND PHARMACODYNAMICS OF SINGLE AND/OR MULTIPLE INTRAVENOUS AND/OR SUBCUTANEOUS DOSES OF PF-06817024 IN HEALTHY SUBJECTS WHO MAY BE MILDLY ATOPIC, SUBJECTS WITH CHRONIC RHINOSINUSITIS WITH NASAL POLYPS, AND SUBJECTS WITH MODERATE-SEVERE ATOPIC DERMATITIS

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Trial Profile

A PHASE 1, RANDOMIZED, DOUBLE-BLIND, THIRD-PARTY OPEN, PLACEBO-CONTROLLED, DOSE ESCALATING STUDY TO EVALUATE THE SAFETY, TOLERABILITY, PHARMACOKINETICS AND PHARMACODYNAMICS OF SINGLE AND/OR MULTIPLE INTRAVENOUS AND/OR SUBCUTANEOUS DOSES OF PF-06817024 IN HEALTHY SUBJECTS WHO MAY BE MILDLY ATOPIC, SUBJECTS WITH CHRONIC RHINOSINUSITIS WITH NASAL POLYPS, AND SUBJECTS WITH MODERATE-SEVERE ATOPIC DERMATITIS

Status: Completed
Phase of Trial: Phase I

Latest Information Update: 23 May 2022

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At a glance

  • Drugs PF 06817024 (Primary) ; PF 06817024 (Primary)
  • Indications Atopic dermatitis; Nasal polyps; Rhinosinusitis
  • Focus Adverse reactions
  • Sponsors Pfizer

    • Most Recent Events

    • 11 Apr 2021 Status changed from active, no longer recruiting to completed.
    • 04 Feb 2019 Planned End Date changed from 15 Feb 2021 to 14 Feb 2021.
    • 04 Feb 2019 Planned primary completion date changed from 15 Feb 2021 to 14 Feb 2021.

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