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
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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