drugset / Trial / NCT07222709

A Study to Assess the Adverse Events and How Oral ABBV-1042 Moves Through the Body of Healthy Adult Participants

NCT07222709 ↗

Phase 1 Recruiting 48 enrolled AbbVie
RandomizedSequentialTriple-blindBasic science

Summary

This study will assess the adverse events, tolerability, and how oral ascending doses of ABBV-1042 moves through the body of healthy adult participants.

Timeline

Start
2025-10-27
Primary completion
2026-05
Completion
2026-05

Drugs

EvaluationDrugModalityDoseRoute
Subject ABBV-1042 Unknown — Oral

Indications

No indication recorded.