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
Latest Information Update: 30 Jul 2026
At a glance
- Drugs ABBV 722 (Primary)
- Indications Unspecified
- Focus Adverse reactions; First in man; Pharmacokinetics
- Sponsors AbbVie
Most Recent Events
- 27 Jul 2026 Status changed from active, no longer recruiting to completed.
- 25 Jun 2026 Planned End Date changed from 1 Apr 2026 to 1 Jun 2026.
- 25 Jun 2026 Planned primary completion date changed from 1 Apr 2026 to 1 Jun 2026.