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Study details
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A Study of ABBV-295 Subcutaneous Injections to Assess Adverse Events and Pharmacokinetics in Adult Participants With Obesity

AbbVie
NCT IDNCT07291232ClinicalTrials.gov data as of Apr 2026
Phase

Phase 1

Target enrollment

96

Study length

about 12 months

Ages

18–65

Locations

1 site in IL

What this study is about

This trial is testing a treatment called ABBV-295, given as subcutaneous injections, in adults with obesity. The goal is to see what side effects occur and how the body processes this medication.

Simplified from trial records by PatientMatch.

What you may be asked to do

  • 1.Take ABBV-295
  • 2.Take Placebo

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
Randomized & Blinded

You may get a placebo/standard care, and you won't know which.

Extracted study details

Pulled from the trial record to show what is being tested and what the study is measuring.

Endpoints

Primary: Area under the plasma concentration-time curve (AUC) of ABBV-295, Dose Normalized AUC of ABBV-295, Dose Normalized Cmax of ABBV-295, Incidence of Anti-Drug Antibodies (ADAs), Maximum Observed Plasma Concentration (Cmax) of ABBV-295, Number of Participants with Abnormal Change From Baseline in Vital Sign Measurements, Number of Participants with Adverse Events (AEs), Number of Participants with Change from Baseline in Electrocardiogram (ECG)

Body systems

Endocrinology