A Single Dose Study to Assess Adverse Events and How Oral Icalcaprant Moves Through the Body in Healthy Adult Japanese and Han Chinese Participants

Study Identifier
M25-528
CT.gov Identifier
EudraCT Identifier
Not available
EUCTIS ID
Not available
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Study Complete

Study Details

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

    Protocol Summary

    This study will assess the pharmacokinetics, safety, and tolerability of icalcaprant administered orally in healthy adult Japanese and Han Chinese participants.

    Study Locations

    Location
    Status
    Location
    Anaheim Clinical Trials, LLC /ID# 271323
    Anaheim, California, United States, 92801
    Status
    Not applicable