Skip to content
Study details
Enrolling now

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

About this study

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.

Based on ClinicalTrials.gov records.

What participants do

  • 1.Take ABBV-295
  • 2.Take Placebo
PhasePhase 1
Primary goalArea under the plasma concentration-time curve (AUC) of ABBV-295

Participation effort

Estimated from trial records. Details can vary by site.

Time + visits
Low10%
Logistics
Moderate50%

Logistics difficulty varies by site location and availability.

Trial highlights

Treatment details

Auto-extracted from trial records to preview treatments and outcomes.

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