A Study to Assess the Safety, Tolerability and How Single Ascending Doses of ABBV-859 Moves Through the Body of Healthy Adult Participants
Part of paid clinical trials in Anaheim, California.
- Sponsor
- AbbVie
- Study ID
- NCT07736638
- Phase
- PHASE1
- Status
- Recruiting
Conditions
- Healthy Volunteer
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - 65 Years
- Healthy Volunteers
- Accepted
Interventions
- ABBV-859 — DRUGOral Tablet
- Placebo for ABBV-859 — DRUGOral Tablet
- ABBV-859 — DRUGIntravenous (IV) Infusion
- Placebo for ABBV-859 — DRUGIntravenous (IV) Infusion
Study Details
The objective of this study is to assess the pharmacokinetic (PK), immunogenicity, safety, and tolerability of ABBV-859 after single ascending doses in healthy adult volunteers.
Key Dates
- First listed
- Jul 30, 2026
- Start date
- Jul 28, 2026
- Status verified
- Jul 2026
- Primary completion
- Feb 28, 2027
- Completion
- Feb 28, 2027
Study Design
- Enrollment
- 64 participants (estimated)
- Allocation
- RANDOMIZED
- Intervention model
- SEQUENTIAL
- Primary purpose
- TREATMENT
Arms
- Experimental: Group 1Participants will receive either ABBV-859 single Dose A, or the Placebo equivalent, on Study Day 1
- Experimental: Group 2Participants will receive either ABBV-859 single Dose B, or the Placebo equivalent, on Study Day 1
- Experimental: Group 3Participants will receive either ABBV-859 single Dose C, or the Placebo equivalent, on Study Day 1
- Experimental: Group 4Participants will receive either ABBV-859 single Dose D, or the Placebo equivalent, on Study Day 1
- Experimental: Group 5Participants will receive either ABBV-859 single Dose E, or the Placebo equivalent, on Study Day 1
- Experimental: Group 6Participants will receive either ABBV-859 single Dose F, or the Placebo equivalent, on Study Day 1
- Experimental: Group 7Participants will receive either ABBV-859 single Dose G, or the Placebo equivalent, on Study Day 1
- Experimental: Group 8Participants will receive either ABBV-859 single Dose H, or the Placebo equivalent, on Study Day 1
Primary Outcome Measure
Number of Participants with Adverse Events (AEs) [ Time Frame: Up to 99 Days ]
Central Contacts
- ABBVIE CALL CENTER844-663-3742
Locations (2)
| Facility | City | State | ZIP | Site coordinators |
|---|---|---|---|---|
| CenExel ACT- Anaheim Clinical Trials /ID# 284382 | Anaheim | California | 92801 | - |
| Acpru /Id# 284029 | Grayslake | Illinois | 60030 | - |
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