drugset / Trial / NCT03383276
Phase 1 Study for Safety and Tolerability of IL-1-Ra Topically Administered to Eyes of Healthy Adult Subjects
Phase 1
Unknown
34 enrolled
Beijing Tongren Hospital
Chengdu Rhodiola Bio-Pharmaceutical Co Ltd · collab
SequentialOpen-labelTreatment
Summary
The purpose of this study is to assess the safety and tolerability of ocular administration of Topical Interleukin-1-Receptor Antagonist in healthy volunteers. Additionally, the PK of Interleukin-1-Receptor Antagonist will be assessed.
Timeline
- Start
- 2017-12-18
- Primary completion
- 2018-03-25
- Completion
- 2018-06-10
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | IL-1Ra | Unknown | — | Topical |