drugset / Trial / NCT03131648

Tralokinumab Monotherapy for Moderate to Severe Atopic Dermatitis - ECZTRA 1 (ECZema TRAlokinumab Trial no. 1)

NCT03131648 ↗

Phase 3 Completed 802 enrolled LEO Pharma
RandomizedParallel-groupDouble-blindTreatment

Summary

Primary objective: To evaluate the efficacy of tralokinumab compared with placebo in treating moderate to severe atopic dermatitis (AD). Secondary objectives: To evaluate the efficacy of tralokinumab on severity and extent of AD, itch, and health related quality of life compared with placebo. Maintenance objective: To evaluate maintenance of effect with continued tralokinumab dosing up to 52 weeks compared to placebo for subjects achieving clinical response at Week 16.

Timeline

Start
2017-05-30
Primary completion
2018-08-07
Completion
2019-10-10

Outcome

Met primary endpoint

registry analysis (superiority test); Tralokinumab 300 mg Q2W vs Placebo Q2W; p = 0.002; Risk Difference (RD) 8.6 (95% CI 4.1 to 13.1) NCT03131648 ↗

registry analysis (superiority test); Tralokinumab 300 mg Q2W vs Placebo Q2W; p <0.001; Risk Difference (RD) 12.1 (95% CI 6.5 to 17.7) NCT03131648 ↗

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Tralokinumab Monoclonal antibody 300 mg Subcutaneous

Indications