drugset / Trial / NCT06078202

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

NCT06078202 ↗

Phase 1 Withdrawn AbbVie
RandomizedSequentialOpen-labelTreatment

Summary

The purpose of this study is to evaluate the relative bioavailability of three immediate-release table formulations of ABBV-903 under fasting conditions in healthy volunteers, and to evaluate the effect of food on the pharmacokinetics of three immediate-release table formulations of ABBV-903.

Timeline

Start
2024-12-01
Primary completion
2025-01-31
Completion
2025-01-31

Outcome

Outcome not reported

Stopped (Business): “Strategic considerations”

Drugs

EvaluationDrugModalityDoseRoute
Subject ABBV-903 Unknown — Oral

Indications

No indication recorded.