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
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
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | ASLAN004 | Monoclonal antibody | 200 mg | Subcutaneous |
| Subject | ASLAN004 | Monoclonal antibody | 400 mg | Subcutaneous |
| Subject | ASLAN004 | Monoclonal antibody | 600 mg | Subcutaneous |