TerminatedPhase 3NCT04611152
A Trial to Evaluate the Efficacy, Durability, and Safety of KSI-301 Compared to Aflibercept in Participants With Diabetic Macular Edema (DME)
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
- 460 target
- Eligibility
- 18 years · All sexes
- Timeline
- 2020 – 2023
Study locations (30)
- UCSD Jacobs Retina Center, La Jolla, California, United States
- Retina Consultants of Southern California, Redlands, California, United States
- California Retina Consultants, Santa Maria, California, United States
- Lundquist Institute for Biomedical Innovation at Harbor-UCLA Medical Center, Torrance, California, United States
- Colorado Retina Associates PC, Lakewood, Colorado, United States
- Conneticut Eye Consultants, Danbury, Connecticut, United States
- Retina Group of Florida, Boca Raton, Florida, United States
- Blue Ocean Clinical Research, Clearwater, Florida, United States
- Vitreo Retinal Associates, Gainesville, Florida, United States
- Florida Retina Consultants, Lakeland, Florida, United States
- Florida Eye Associates, Melbourne, Florida, United States
- Florida Retina Institute, Orlando, Florida, United States
- Retina Specialty Institute, Pensacola, Florida, United States
- Retina Associates of Florida, Tampa, Florida, United States
- Retina Vitreous Associates of Florida, Tampa, Florida, 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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