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Arm 1: Healthy Japanese Participants for Healthy Subjects

Phase 1
Waitlist Available
Research Sponsored by AbbVie
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
Be between 18 and 65 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up up to approximately 45 days
Awards & highlights

Summary

This trial will assess safety and how ABBV-552 moves through the body of 18 adult healthy Japanese & Han Chinese volunteers. Adverse Events will be monitored.

Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~up to approximately 45 days
This trial's timeline: 3 weeks for screening, Varies for treatment, and up to approximately 45 days for reporting.

Treatment Details

Study Objectives

Outcome measures can provide a clearer picture of what you can expect from a treatment.
Primary outcome measures
AUC From Time Zero to Infinite Time (AUCinf) of ABBV-552
AUC of ABBV-552 (Arm 1)
Apparent Oral Clearance (CL/F) of ABBV-552
+8 more

Trial Design

2Treatment groups
Experimental Treatment
Group I: Arm 2: Healthy Han Chinese ParticipantsExperimental Treatment1 Intervention
Participants will receive ABBV-552 once a week for 7 Days.
Group II: Arm 1: Healthy Japanese ParticipantsExperimental Treatment1 Intervention
Participants will receive ABBV-552 once a week for 21 Days.
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
ABBV-552
2023
Completed Phase 1
~30

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Logistics

Participation is compensated

You will be compensated for participating in this trial.

Who is running the clinical trial?

AbbVieLead Sponsor
983 Previous Clinical Trials
509,343 Total Patients Enrolled
ABBVIE INC.Study DirectorAbbVie
414 Previous Clinical Trials
151,874 Total Patients Enrolled
~7 spots leftby Jul 2025
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