A Study to Evaluate the Safety, Tolerability, Pharmacokinetics, and Immunogenicity of Single Ascending Subcutaneous or Intravenous Doses of ABBV-701 in Healthy Adult Western and Asian Participants

Study Identifier
M25-491
CT.gov Identifier
EudraCT Identifier
Not available
EUCTIS ID
Not available
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Study Details

Medical Condition
  • Healthy Volunteer
  • Study Drug
  • ABBV-701
  • Placebo
  • Phase
    Phase 1
    Sex
    Female & Male
    Age
    18 - 60 Years

    Protocol Summary

    The main objective of this study is to assess the safety, tolerability, pharmacokinetics, and immunogenicity of single ascending doses of ABBV-701 in healthy adult western and Asian participants.

    Study Locations

    Location
    Status
    Location
    CenExel ACT- Anaheim Clinical Trials /ID# 278431
    Anaheim, California, United States, 92801
    Status
    Not applicable
    Location
    Acpru /Id# 273354
    Grayslake, Illinois, United States, 60030
    Status
    Not applicable