drugset / Trial / NCT05442788
A Study of HB0017 in Patients With Moderate to Severe Plaque Psoriasis
RandomizedParallel-groupQuadruple-blindTreatment
Summary
This is a randomized, double-blind, placebo-controlled, dose-escalation Phase Ib study to evaluate the safety, tolerability, and pharmacokinetics of HB0017 following multiple dose in patients with moderate to severe plaque psoriasis.
Timeline
- Start
- 2021-09-02
- Primary completion
- 2022-05-31
- Completion
- 2022-05-31
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | HB0017 | Monoclonal antibody | 150 mg | Subcutaneous |
| Subject | HB0017 | Monoclonal antibody | 300 mg | Subcutaneous |
| Subject | HB0017 | Monoclonal antibody | 450 mg | Subcutaneous |