drugset / Trial / NCT04090229

A Multi-center, Randomized, Double-blind, Placebo-controlled, Multiple Ascending Dose Study of the Safety, Tolerability, and Pharmacokinetics of Subcutaneously Delivered ASLAN004 in Adults With Moderate-Severe Atopic Dermatitis

NCT04090229 ↗

Phase 1 Completed 52 enrolled ASLAN Pharmaceuticals
RandomizedParallel-groupQuadruple-blindTreatment

Summary

A Phase 1B, multi-center, double-blind, placebo-controlled, randomized, multiple ascending dose (MAD) clinical study is designed to evaluate ASLAN004 versus placebo in patients who have moderate-severe AD. The treatment period duration will be 8 weeks with a 12-week follow-up period after the end of treatment.

Timeline

Start
2019-09-09
Primary completion
2021-10-28
Completion
2021-12-03

Drugs

EvaluationDrugModalityDoseRoute
Subject ASLAN004 Monoclonal antibody 200 mg Subcutaneous
Subject ASLAN004 Monoclonal antibody 400 mg Subcutaneous
Subject ASLAN004 Monoclonal antibody 600 mg Subcutaneous

Indications