drugset / Trial / NCT05180526
Assessment of Safety , Clinical Efficacy with QLETLI in Non-infectious Uveitis (UV)
NaSingle-groupOpen-labelTreatment
Summary
This is a multicenter, prospective, post-marketing clinical study with a total of 60 uveitis (UV) subjects planned to be enrolled. Screening period (-2\~0 weeks) ,Treatment period (1-22 weeks), Follow-up period, At the same time, plasma concentration will be determined
Timeline
- Start
- 2021-12-27
- Primary completion
- 2024-12-30
- Completion
- 2024-12-30
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | QLETLI | Unknown | 40 mg | Subcutaneous |