drugset / Trial / NCT05283694

A Study to Evaluate the Bioavailability of Risankizumab Following Subcutaneous Dosing in Healthy Male Participants

NCT05283694

Phase 1 Completed 48 enrolled AbbVie
RandomizedParallel-groupOpen-labelBasic science

Summary

The objective of this study is to evaluate the bioavailability, safety and tolerability of risankizumab following subcutaneous injections in healthy male participants.

Timeline

Start
2017-09-11
Primary completion
2018-06-12
Completion
2018-06-12

Drugs

EvaluationDrugModalityDoseRoute
Subject Risankizumab Monoclonal antibody Subcutaneous

Indications

No indication recorded.