Clinical Trials Directory

Trials / Unknown

UnknownNCT03383276

Phase 1 Study for Safety and Tolerability of IL-1-Ra Topically Administered to Eyes of Healthy Adult Subjects

A Phase 1, Dose Escalating Study of the Safety, Tolerability, and Pharmacokinetics of IL-1-Ra Topically Administered to Eyes of Healthy Adult Subjects

Status
Unknown
Phase
Phase 1
Study type
Interventional
Enrollment
34 (estimated)
Sponsor
Beijing Tongren Hospital · Academic / Other
Sex
All
Age
18 Years – 45 Years
Healthy volunteers
Accepted

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.

Conditions

Interventions

TypeNameDescription
DRUGIL-1Racustom eye drop to be applied to the left eye.

Timeline

Start date
2017-12-18
Primary completion
2018-03-25
Completion
2018-06-10
First posted
2017-12-26
Last updated
2017-12-26

Locations

1 site across 1 country: China

Source: ClinicalTrials.gov record NCT03383276. Inclusion in this directory is not an endorsement.