LivingGLP1
Study S003321

A PHASE 1, OPEN-LABEL, MULTIPLE DOSE STUDY TO INVESTIGATE THE IMPACT OF PF 08653944 ON GASTRIC EMPTYING IN ADULT PARTICIPANTS WITH OVERWEIGHT OR OBESITY

Registration

Registration
NCT07508241
Study type
INTERVENTIONAL
Phase
PHASE1
Masking
NONE
Status
ACTIVE_NOT_RECRUITING
Enrollment
22
Start
2026-03-31
Primary completion
2027-01-27
Lead sponsor
Pfizer
Conditions
Obesity; Overweight and/or Obesity; Overweight; Drug Interaction
Interventions
DRUG:PF-08653944; DRUG:Acetaminophen
Results posted
FALSE
Individual participant data sharing
NO
Secondary identifiers
OTHER:MET097-25-106

Registered primary outcomes

  • Acetaminophen Pharmacokinetic (PK) Parameters: Maximum observed plasma concentration (Cmax) [Day 1 pre-dose through approximately 11 Weeks after last dose of study intervention.]
  • Acetaminophen PK parameters: Area under the plasma concentration (AUC) [Day 1 pre-dose through approximately 11 Weeks after last dose of study intervention.]
  • Acetaminophen PK parameters: Time to Maximum concentration (Tmax) [Day 1 pre-dose through approximately 11 Weeks after last dose of study intervention.]

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