drugset / Trial / NCT05283681

A Study to Evaluate the Bioavailability of Risankizumab in Pre-filled Syringe or Auto-injector in Healthy Adult Participants

NCT05283681

Phase 1 Completed 226 enrolled AbbVie
RandomizedParallel-groupOpen-labelBasic science

Summary

The objective of this study is to evaluate the bioavailability of risankizumab new formulation in prefilled syringe (PFS) relative to the 90 mg/mL formulation in PFS in healthy volunteers. The study will also evaluate the bioavailability of risankizumab new formulation in auto-injector (AI) relative to PFS in healthy volunteers.

Timeline

Start
2019-04-02
Primary completion
2019-11-11
Completion
2019-11-11

Drugs

EvaluationDrugModalityDoseRoute
Subject Risankizumab Monoclonal antibody Subcutaneous

Indications

No indication recorded.