CompletedPhase 3NCT04592419
A Study to Evaluate the Efficacy, Durability, and Safety of KSI-301 Compared to Aflibercept in Patients With Macular Edema Due to Retinal Vein Occlusion (RVO)
Studying Central retinal vein occlusion
Last synced from ClinicalTrials.gov
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Clinical trial records are synced from ClinicalTrials.gov through automated extraction.
Report missing dataKey facts
- Sponsor
- Kodiak Sciences Inc
- Principal Investigator
- Pablo Velazquez-Martin, MDKodiak Sciences Inc
- Intervention
- KSI-301(drug)
- Enrollment
- 568 enrolled
- Eligibility
- 18 years · All sexes
- Timeline
- 2020 – 2023
Study locations (30)
- Northwest Arkansas Retina Associates, Phoenix, Arizona, United States
- Retinal Research Institute, LLC, Phoenix, Arizona, United States
- Retina Vitreous Associates, Beverly Hills, California, United States
- Eye Medical Center of Fresno, Fresno, California, United States
- Retina Consultants of Orange County, Fullerton, California, United States
- UCSD Jacobs Retina Center, La Jolla, California, United States
- Northern California Retina Vitreous Associates, Mountain View, California, United States
- Retina Consultants of San Diego, Poway, California, United States
- Retina Consultants of Southern California, Redlands, California, United States
- Retinal Consultants Medical Group Inc, Sacramento, California, United States
- Orange County Retina Medical Group, Santa Ana, California, United States
- California Retina Consultants, Santa Maria, California, United States
- Colorado Retina Associates PC, Lakewood, Colorado, United States
- Conneticut Eye Consultants, Danbury, Connecticut, United States
- Retina Group of New England, Waterford, Connecticut, United States
- +15 more locations on ClinicalTrials.gov
Primary source
Recruitment status, site addresses, contacts, and full eligibility criteria can change between syncs. Always verify with the trial team before planning travel or treatment.
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