MedPath

A Phase 3 Study to Evaluate the Efficacy and Safety of Intravitreal KSI-101 in Participants With Macular Edema Secondary to Inflammation (MESI) - PEAK

Phase 3
Not yet recruiting
Conditions
Macular Edema Secondary to Inflammation
Interventions
Other: Sham Comparator
Registration Number
NCT06990399
Lead Sponsor
Kodiak Sciences Inc
Brief Summary

A Phase 3 Study to Evaluate the Efficacy and Safety of Intravitreal KSI-101 in Participants with Macular Edema Secondary to Inflammation (MESI)

Detailed Description

Not available

Recruitment & Eligibility

Status
NOT_YET_RECRUITING
Sex
All
Target Recruitment
150
Inclusion Criteria
  • MESI with a central subfield thickness (CST) of ≥400 microns on SD-OCT in Study Eye.
  • BCVA ETDRS score of ≥25 and ≤70 letters (between 20/40 and 20/320 Snellen equivalent) in the Study Eye.
  • Diagnosis of active or inactive non-infectious intraocular inflammation, acute or chronic in the Study Eye.
Exclusion Criteria
  • ME in the Study Eye secondary to diabetes, RVO, or wAMD
  • Active or suspected ocular or periocular infection in either eye

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
KSI-101 10 mgKSI-101Intravitreal injection of KSI-101 10 mg once every 4 weeks for 6 monthly doses followed by individualized dosing
ShamSham ComparatorSham injection once every 4 weeks for 6 monthly doses followed by individualized sham dosing
KSI-101 5 mgKSI-101Intravitreal injection of KSI-101 5 mg once every 4 weeks for 6 monthly doses followed by individualized dosing
Primary Outcome Measures
NameTimeMethod
Mean change in BCVAWeek 24

Mean change in BCVA from Day 1 to the average of Week 20 and Week 24.

Secondary Outcome Measures
NameTimeMethod
© Copyright 2025. All Rights Reserved by MedPath