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A PHASE 1, OPEN- LABEL STUDY TO EVALUATE THE MULTIPLE DOSE PHARMACOKINETICS OF DANUGLIPRON FOLLOWING ORAL ADMINISTRATION IN OTHERWISE HEALTHY ADULT PARTICIPANTS WITH OVERWEIGHT OR OBESITY
The purpose of this study is to learn the following about the study medicine, danuglipron, after multiple days of dosing in healthy adults who are overweight or obese: * how the study medicine, danuglipron, is taken up into the blood * about the safety and tolerability of danuglipron The total number of weeks of the study is about 15 (about 4 months).
Age
18 - No limit years
Sex
ALL
Healthy Volunteers
Yes
Pfizer Clinical Research Unit - New Haven
New Haven, Connecticut, United States
Start Date
August 23, 2024
Primary Completion Date
December 18, 2024
Completion Date
December 18, 2024
Last Updated
January 20, 2025
23
ACTUAL participants
Danuglipron
DRUG
Lead Sponsor
Pfizer
NCT01143454
NCT07472881
Data Source & Attribution
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