drugset / Trial / NCT03591887
A Study to Evaluate ABY-035 in Subjects With Moderate-to-severe Plaque Psoriasis
RandomizedParallel-groupQuadruple-blindTreatment
Summary
This randomized, double-blinded dose-finding study evaluates four dose levels of ABY-035, in comparison to placebo, in subjects with moderate to severe plaque psoriasis. The study consists of 52-week Core study and two optional 52-week periods, Extension and Prolongation of Extension. The Core study consists of three periods: Induction (placebo-controlled, Week 0-12), Optimization (Week 12-24), and Individualization (Week 24-52).
Timeline
- Start
- 2018-03-07
- Primary completion
- 2019-03-27
- Completion
- 2021-12-03
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Izokibep | Protein / enzyme biologic | 2 mg | Subcutaneous |
| Subject | Izokibep | Protein / enzyme biologic | 20 mg | Subcutaneous |
| Subject | Izokibep | Protein / enzyme biologic | 80 mg | Subcutaneous |
| Subject | Izokibep | Protein / enzyme biologic | 160 mg | Subcutaneous |