drugset / Trial / NCT04674826

A Trial to Compare the Pharmacokinetics of Tralokinumab in Healthy Subjects

NCT04674826

Phase 1 Completed 101 enrolled LEO Pharma
RandomizedCrossoverOpen-labelTreatment

Summary

The purpose of this trial is to compare the pharmacokinetics (PK), safety, tolerability and immunogenicity of a single dose of 300 mg tralokinumab administered as a 1 × X mL subcutaneous (SC) injection with Device A and 2 × Y mL consecutive SC injections with Device B.

Timeline

Start
2021-02-08
Primary completion
2021-12-29
Completion
2021-12-29

Drugs

EvaluationDrugModalityDoseRoute
Subject Tralokinumab Monoclonal antibody 300 mg Subcutaneous

Indications

No indication recorded.