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A First-In-Human Study to Evaluate the Pharmacokinetics, Safety, and Tolerability of ABBV-722 Following Single and Multiple Ascending Doses in Healthy Adult Subjects and Single Doses in Healthy Adult Asian Subjects

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Trial Profile

A First-In-Human Study to Evaluate the Pharmacokinetics, Safety, and Tolerability of ABBV-722 Following Single and Multiple Ascending Doses in Healthy Adult Subjects and Single Doses in Healthy Adult Asian Subjects

Status: Recruiting
Phase of Trial: Phase I

Latest Information Update: 06 Aug 2025

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At a glance

  • Drugs ABBV 722 (Primary)
  • Indications Unspecified
  • Focus Adverse reactions; First in man; Pharmacokinetics
  • Sponsors AbbVie

Most Recent Events

  • 20 Jul 2025 Planned number of patients changed from 88 to 96.
  • 20 Jul 2025 Planned End Date changed from 4 Jul 2025 to 1 Apr 2026.
  • 20 Jul 2025 Planned primary completion date changed from 4 Jul 2025 to 1 Apr 2026.

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