drugset / Trial / NCT06774313

A Study to Assess the Adverse Events and How Subcutaneous (SC) Injections and Intravenous (IV) Infusions of ABBV-142 Move Through the Body of Healthy Adult Participants

NCT06774313 ↗

Phase 1 Completed 73 enrolled AbbVie
RandomizedSequentialQuadruple-blindBasic science

Summary

This study is designed to assess the pharmacokinetic properties, safety, tolerability, and immunogenicity of ABBV-142 and determine whether predicted efficacious exposures can be safely achieved in humans.

Timeline

Start
2025-01-22
Primary completion
2026-04-08
Completion
2026-04-08

Drugs

EvaluationDrugModalityDoseRoute
Subject ABBV-142 Unknown — Intravenous

Indications

No indication recorded.