drugset / Trial / NCT06148181

A Study to Evaluate Adverse Events and How Single Ascending Doses of ABBV-141 Move Through the Body of Healthy Adult Western and Asian Participants

NCT06148181 ↗

Phase 1 Completed 41 enrolled AbbVie
RandomizedSequentialDouble-blindBasic science

Summary

The purpose of this study is to assess the safety, tolerability, pharmacokinetics (PK) and immunogenicity after single ascending doses (SAD) of ABBV-141 in healthy adult Western and Asian participants.

Timeline

Start
2024-01-29
Primary completion
2024-12-30
Completion
2024-12-30

Drugs

EvaluationDrugModalityDoseRoute
Subject ABBV-141 Unknown — Intravenous

Indications

No indication recorded.