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 — DRUG
    Oral Tablet
  • Placebo for ABBV-859 — DRUG
    Oral Tablet
  • ABBV-859 — DRUG
    Intravenous (IV) Infusion
  • Placebo for ABBV-859 — DRUG
    Intravenous (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 1
    Participants will receive either ABBV-859 single Dose A, or the Placebo equivalent, on Study Day 1
  • Experimental: Group 2
    Participants will receive either ABBV-859 single Dose B, or the Placebo equivalent, on Study Day 1
  • Experimental: Group 3
    Participants will receive either ABBV-859 single Dose C, or the Placebo equivalent, on Study Day 1
  • Experimental: Group 4
    Participants will receive either ABBV-859 single Dose D, or the Placebo equivalent, on Study Day 1
  • Experimental: Group 5
    Participants will receive either ABBV-859 single Dose E, or the Placebo equivalent, on Study Day 1
  • Experimental: Group 6
    Participants will receive either ABBV-859 single Dose F, or the Placebo equivalent, on Study Day 1
  • Experimental: Group 7
    Participants will receive either ABBV-859 single Dose G, or the Placebo equivalent, on Study Day 1
  • Experimental: Group 8
    Participants 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

Locations (2)

FacilityCityStateZIPSite coordinators
CenExel ACT- Anaheim Clinical Trials /ID# 284382AnaheimCalifornia92801-
Acpru /Id# 284029GrayslakeIllinois60030-

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