A Study to Assess the Adverse Events and How Subcutaneous (SC) Injections and Intravenous (IV) Infusions of ABBV-142 Move Through the Body of Healthy Adult Participants

Study Identifier
M25-265
CT.gov Identifier
EudraCT Identifier
Not available
EUCTIS ID
Not available
For general inquiries, please contact
Study Complete

Study Details

Medical Condition
  • Healthy Volunteer
  • Study Drug
  • ABBV-142
  • Placebo
  • Phase
    Phase 1
    Sex
    Female & Male
    Age
    18 - 55 Years

    Protocol Summary

    This study is designed to assess the pharmacokinetic properties, safety, tolerability, and immunogenicity of ABBV-142 and determine whether predicted efficacious exposures can be safely achieved in humans.

    Study Locations

    Location
    Status
    Location
    Acpru /Id# 271899
    Grayslake, Illinois, United States, 60030
    Status
    Not applicable