About this trial
The objective of this study is to assess the safety, tolerability, pharmacokinetics, and immunogenicity of single and multiple doses of ABBV-313 in healthy adult participants.
Eligibility criteria
Qualifiers
BMI is >= 18.0 to <= 29.9 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.
A condition of general good health, based upon the results of a medical history, physical examination, vital signs, laboratory profile and a 12-lead ECG.
Disqualifiers
History of any clinically significant sensitivity or allergy to any medication or food.
History of any clinically significant illness/infection/major febrile illness, hospitalization, or any surgical procedure within 30 days prior to the first dose of study treatment.
Participant has prior exposure to ABBV-313 within the past 300 days.
Trial design
Treatments tested in this trial
- ABBV-313
- Placebo
- ABBV-313
- Placebo
Treatment groups
8
Treatment groupsSee each treatment group below.
Locations
1Sponsors and collaborators
AbbVie
Lead sponsor