A Study of ABBV-313 in Healthy Adults
This study is looking for healthy adult volunteers to help us understand a new investigational drug called ABBV-313. We want to learn about its safety, how well your body tolerates it, and how your body processes it. Some participants will receive ABBV-313 as an injection or infusion, while others will receive a placebo (an inactive substance that looks like the study drug). We'll be checking for any side effects and measuring how much ABBV-313 is in your blood over time. You can join if you are between 18 and 55 years old, in good general health, and have a BMI (Body Mass Index) between 18.0 and 29.9. The study plans to enroll 64 participants, but its current recruitment status is unclear.
- Study design
- This interventional study plans to enroll 64 healthy adult participants. Some will receive ABBV-313 and others will receive a placebo, either as an injection or an infusion.
- What's involved
- Not specified in the trial record.
- Compensation
- Not stated in the trial record.
- Follow-up
- Participants will be followed for safety and drug levels for up to approximately 329 days.
AI-generated from the public study record. Only the study team can confirm whether you're eligible — confirm details with them before making decisions.
A Study to Assess Safety, Tolerability, and How Single and Multiple Injections or Infusions of ABBV-313 Affects the Body of Adult Participants
At a glance
Conditions
Where it's being run
1 sites across 1 statesStudy leadership
- ABBVIE INC. · STUDY_DIRECTOR · AbbVie
Who to contact
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Do you actually qualify for this trial?
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Inclusion
Exclusion
What this trial measures
- Number of Participants with Adverse Events (AEs)Up to Approximately Day 329
An AE is defined as any untoward medical occurrence in a patient or clinical investigation in which a participant is administered a pharmaceutical product which does not necessarily have a causal relationship with this treatment.
- Maximum Observed Plasma Concentration (Cmax) of ABBV-313Up to Approximately Day 329
Cmax of ABBV-313.
- Time to Cmax (Tmax) of ABBV-313Up to Approximately Day 329
Tmax of ABBV-313.
- Terminal Phase Elimination Rate Constant (Beta) of ABBV-313Up to Approximately Day 329
Beta of ABBV-313.
- Terminal Phase Elimination Half-Life (t1/2) of ABBV-313Up to Approximately Day 329
t1/2 of ABBV-313.
- Area Under the Plasma Concentration-Time Curve (AUC) From Time 0 to the Time of the Last Measurable Concentration (AUCt) of ABBV-313Up to Approximately Day 329
AUCt of ABBV-313.