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Study to Learn About How the Study Medicines Called PF-07976016 and PF-06882961 Are Taken Up by the Body, and if Either of Them Change How the Body Processes the Other Medicine in Otherwise Healthy Adults With Overweight or Obesity

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NCT06910839

Sponsored by Pfizer (industry) · PFE — their whole pipeline →.

Phase
Phase 1
Status
Terminated
Study type
Interventional
Design
Na · None · Basic science
Enrollment
21actual
Sites
1
Country
United States

Every value on this page is a field the sponsor filed with ClinicalTrials.gov, reproduced. Dates are their own estimates, revised as a study runs, unless the registry marks them actual. sources →

Source: ClinicalTrials.gov, retrieved 2026-08-19

Why the sponsor stopped it

The sponsor has made the decision to discontinue development of danuglipron (PF-06882961). As such, this study was discontinued prior to PF-06882961 administration.

As filed on the registry record, in the sponsor's own words.

Dates

each axis at the precision it was filed, with the registry's own basis
DateFiledBasisWhat it is
Start2025-03-13actualWhen the study began enrolling
Primary completion2025-05-01actualThe date the last participant is measured for the primary outcome — the readout window
Study completion2025-05-20actualThe whole study's end, after follow-up
First posted2025-04-04actualWhen this record first appeared on the registry
Results postedWhen the sponsor posted results to the registry
Record updated2025-08-07actualThe sponsor's own last edit to this record — every projection above is as current as this date

What it studies

Conditions

  • Overweight
  • Obesity

Interventions

  • Drug: PF-07976016
  • Drug: PF-06882961

Primary outcomes

what the primary-completion date above is the date OF
Steady state area under the concentration-time profile for PF-07976016
measured From 0 Hours to 24 Hours following steady-state dose
Steady state maximum observed concentration (Cmax) for PF-07976016
measured From 0 Hours to 24 Hours following steady-state dose
Steady state area under the concentration-time profile danuglipron
measured From 0 Hours to 24 Hours following steady-state dose
Steady state maximum observed concentration (Cmax) for danuglipron
measured From 0 Hours to 24 Hours following steady-state dose

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