drugset / Trial / NCT06632938

A Study to Evaluate Adverse Events and How the Drug Moves Through the Body From Subcutaneous (SC) and Intravenous (IV) Doses of ABBV-382 in Healthy Adult Chinese Volunteers

NCT06632938

Phase 1 Completed 24 enrolled AbbVie
RandomizedSequentialSingle-blindTreatment

Summary

The main objectives of this study are to evaluate the safety, tolerability, pharmacokinetics, and immunogenicity of single subcutaneous (SC) and intravenous (IV) doses of ABBV-382 in healthy adult Chinese volunteers.

Timeline

Start
2024-10-08
Primary completion
2025-05-15
Completion
2025-05-15

Drugs

EvaluationDrugModalityDoseRoute
Subject Trosunilimab Monoclonal antibody Subcutaneous

Indications

No indication recorded.