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A 2-PART, PHASE 1, OPEN LABEL STUDY WITH A 4-PERIOD, 4-SEQUENCE, CROSSOVER DESIGN IN COHORT 1 AND A 2-PERIOD, 2-SEQUENCE CROSSOVER DESIGN IN COHORT 2 TO COMPARE THE SINGLE DOSE PHARMACOKINETICS OF FIVE DIFFERENT FORMULATIONS OF PF-06882961 ADMINISTERED ORALLY TO OTHERWISE HEALTHY ADULT PARTICIPANTS WHO ARE OVERWEIGHT OR HAVE OBESITY

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Trial Profile

A 2-PART, PHASE 1, OPEN LABEL STUDY WITH A 4-PERIOD, 4-SEQUENCE, CROSSOVER DESIGN IN COHORT 1 AND A 2-PERIOD, 2-SEQUENCE CROSSOVER DESIGN IN COHORT 2 TO COMPARE THE SINGLE DOSE PHARMACOKINETICS OF FIVE DIFFERENT FORMULATIONS OF PF-06882961 ADMINISTERED ORALLY TO OTHERWISE HEALTHY ADULT PARTICIPANTS WHO ARE OVERWEIGHT OR HAVE OBESITY

Status: Completed
Phase of Trial: Phase I

Latest Information Update: 11 Apr 2022

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At a glance

  • Drugs Danuglipron (Primary)
  • Indications Obesity
  • Focus Pharmacokinetics
  • Sponsors Pfizer

    • Most Recent Events

    • 28 Jul 2021 Status changed from recruiting to completed.
    • 04 Mar 2021 Planned number of patients changed from 16 to 32.
    • 04 Mar 2021 Planned End Date changed from 18 Feb 2021 to 28 May 2021.

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