A 26-Week 2-Part Study to Evaluate the Efficacy and Safety of PF-06882961 in Adults With Obesity

  • End date
    Apr 13, 2022
  • participants needed
  • sponsor
Updated on 19 September 2021
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This study will assess the efficacy, safety, tolerability and pharmacokinetics (PK) of PF-06882961 in adults with obesity. The first part of the study, Part A, consists of study treatment dosing in Weeks 1 to 16. The second part of the study, Part B, is planned such that participants in Part A will continue dosing from Weeks 17 through 26, contingent upon supportive data. The planned End of Treatment is expected to be Week 26. If Part B is not conducted, then End of Treatment will be Week 16.

Condition adiposity, Obesity
Treatment Placebo, PF-06882961
Clinical Study IdentifierNCT04707313
Last Modified on19 September 2021

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