RecruitingAccepts healthy volunteersPhase 1
A Single Ascending Dose, and Food Effect Study of ABBV-7828 in Healthy Adults
AbbVie · NCT07856706
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Key facts
- Compensation
- Not posted. Ask the study team before screening.
- Who can join
- Ages 18–65 · All sexes
- Healthy volunteers
- Accepted
- Study type
- Interventional · Phase 1
- Target enrollment
- 60
- US sites recruiting
- 1
- Study start
- October 2, 2026
- Record last updated
- October 29, 2026
Status re-checked against ClinicalTrials.gov within the last 12 hours.
What the study is about
This study is to evaluate safety, tolerability, pharmacokinetics and effect of food on ABBV-7828 compared to placebo in healthy adult participants.
Being studied: ABBV-7828; Placebo for ABBV-7828
Conditions: Healthy Subjects
Eligibility criteria
Copied from the official record. The study team makes the final decision at screening.
Show full criteria
Inclusion Criteria
- Individuals between 18 to 65 years of age at the time of screening.
- BMI is \<= 18.0 to >= 32.0 kg/m2.
- A condition of general good health, based upon the results of a medical history, physical evaluations, vital signs, laboratory profile and a 12-lead ECG.
Exclusion Criteria
- History of epilepsy, any clinically significant cardiac, respiratory (except mild asthma as a child), renal, hepatic, gastrointestinal, hematologic or psychiatric disease or disorder, or any uncontrolled medical illness.
- Has any clinically significant ECG abnormalities including the following:
- Evidence of 2nd or 3rd degree atrial ventricular (AV) block at screening visit or upon initial confinement
- QT interval corrected for heart rate (QTc) using Fridericia's correction formula (QTcF) > 450 msec (males) or > 460 msec (females) at screening visit or upon initial confinement.
- History of any clinically significant sensitivity or allergy to any medication or food.
- History of or active medical condition(s) or surgical procedure(s) that might affect gastrointestinal motility, pH, or absorption.
Recruiting US locations
Acpru /Id# 283545
Grayslake, IL 60030
Study contacts (from the official record)
- ABBVIE CALL CENTER · 844-663-3742 · abbvieclinicaltrials@abbvie.com
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