ABBV-295 Injections for Adult Obesity

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

Recruiting Phase 1 Interventional Study
Obesity
No Placebo Group Every participant receives an active treatment — no one gets a placebo.
Ready to participate?

Review the details below, then apply to join this clinical trial.

At a Glance
Age
18 – 65
Sex
Any
Trial phase
Phase 1
Study type
Interventional
Purpose
Treatment
Participants needed
80 (estimated)
Sponsor
AbbVie · Industry
Who this trial is looking for

This trial is looking for adults with obesity to test an injection called ABBV-295. Participants will receive either the study treatment or a placebo and will be monitored for any side effects and changes in weight.

Are You a Good Fit for This Trial?

You may be able to join if

  • I have a BMI between 30 and 45
  • I may have weight-related health issues like high blood pressure or sleep apnea
  • I am a female who is not pregnant or breastfeeding
  • I am not planning to get pregnant or donate eggs during the study or for 60 days after

You may not be able to join if

  • I have gained or lost more than 5% of my body weight in the last 3 months
  • My HbA1c level is 6.5% or higher
  • My serum glucose level is 126 mg/dL or higher
  • I have taken medication to treat obesity in the last 180 days
  • I have been in another obesity trial in the last 180 days

Summarized in plain language from this trial's official eligibility criteria. The full criteria are further down this page — only the research team can confirm whether you qualify.

Think this trial could be right for you?

Answer three quick questions written from this study's own rules to see if you may qualify. No account needed to find out.

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About This Trial

This study is to assess adverse events, change in body weight and pharmacokinetics in adult participants with obesity receiving ABBV-295 subcutaneous injections or matching placebo.

Trial Locations
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Eligibility Criteria
Inclusion Criteria: * BMI ≥ 30.0 to ≤ 45.0 kg/m2 after rounding to the tenths decimal at Screening (BMI is calculated as weight in kg divided by the square of height measured in meters) with or without weight related stable comorbidities (e.g., hypertension, dyslipidemia, obstructive sleep apnea, c…
Contacts

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844-663-3742

abbvieclinicaltrials@abbvie.com

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