drugset / Trial / NCT05268068

A Study of Intravenously (IV) Infused or Subcutaneously (SC) Injected Risankizumab in Healthy Adult Participants in China

NCT05268068

Phase 1 Completed 30 enrolled AbbVie
RandomizedParallel-groupOpen-labelBasic science

Summary

The objective of this study to assess the pharmacokinetics, safety, tolerability and immunogenicity following a single subcutaneous (SC) or intravenous (IV) dose of risankizumab in healthy Chinese participants.

Timeline

Start
2019-06-27
Primary completion
2020-04-26
Completion
2020-04-26

Drugs

EvaluationDrugModalityDoseRoute
Subject Risankizumab Monoclonal antibody Intravenous

Indications

No indication recorded.