drugset / Trial / NCT05836506

A Study to Assess the Relative Bioavailability of Immediate Release Formulations of ABBV-903 in Healthy Adult Participants

NCT05836506 ↗

Phase 1 Completed 24 enrolled AbbVie
RandomizedSequentialOpen-labelTreatment

Summary

The main objective of this study is to assess the relative bioavailability and pharmacokinetics of ABBV-903 in healthy adult participants.

Timeline

Start
2023-04-18
Primary completion
2023-06-20
Completion
2023-06-20

Drugs

EvaluationDrugModalityDoseRoute
Subject ABBV-903 Unknown — Oral

Indications

No indication recorded.