Study details
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A Study to Assess Adverse Events, Tolerability, and Pharmacokinetics of Subcutaneous Injections of ABBV-295 in Healthy Adult Japanese Participants With Overweight or Obesity.
AbbVie
NCT IDNCT07514260ClinicalTrials.gov data as of Apr 2026
Phase
Phase 1
Ages
18–65
Locations
1 site in CA
What this study is about
This Phase 1 study is focused on people with healthy volunteers. The primary outcome being measured is Number of Participants with Adverse Events (AEs).
Simplified from trial records by PatientMatch.
Participation Burden
What's physically and logistically required of participants.
Logistics & Travel
In-person visits
Requires travel to a study site
Physical Intervention
Standard
How treatment is administered
Treatment Assignment
Standard assignment
Assignment is predetermined by the study protocol.
Extracted study details
Pulled from the trial record to show what is being tested and what the study is measuring.
Endpoints
Primary: Number of Participants with Adverse Events (AEs)