drugset / Trial / NCT02525094

Phase 2a Study to Evaluate the Efficacy and Safety of MEDI9929 in Adults With Atopic Dermatitis

NCT02525094 ↗

Phase 2 Completed 113 enrolled MedImmune LLC Amgen · collab
RandomizedParallel-groupQuadruple-blindTreatment

Summary

To assess the efficacy and safety of MEDI9929 in adult subjects with Atopic Dermatitis

Timeline

Start
2015-08-15
Primary completion
2016-05-09
Completion
2016-07-15

Outcome

Missed primary endpoint

registry analysis (superiority test); Placebo vs MEDI9929 280 mg; Odds Ratio (OR) 1.97 (95% CI 0.90 to 4.33) NCT02525094 ↗

Drugs

EvaluationDrugModalityDoseRoute
Subject Tezepelumab Monoclonal antibody 280 mg Subcutaneous

Indications