TerminatedPhase 3NCT04603937
A Study 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
ℹ
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
- 459 target
- Eligibility
- 18 years · All sexes
- Timeline
- 2020 – 2023
Study locations (30)
- Retinal Research Institute, LLC, Phoenix, Arizona, United States
- Retina Vitreous Associates, Beverly Hills, California, United States
- Retina Consultants of Orange County, Fullerton, California, United States
- Northern California Retina Vitreous Associates, Mountain View, California, United States
- Retina Consultants of San Diego, Poway, California, United States
- Retinal Consultants Medical Group Inc, Sacramento, California, United States
- Retina Group of New England, Waterford, Connecticut, United States
- Florida Eye Microsurgical Institute, Boynton Beach, Florida, United States
- Rand Eye Institute, Deerfield Beach, Florida, United States
- National Ophthalmic Research Institute, Fort Myers, Florida, United States
- Fort Lauderdale Eye Institute, Plantation, Florida, United States
- Retina Vitreous Associates of Florida, St. Petersburg, Florida, United States
- Southern Vitreoretinal Associates, Tallahassee, Florida, United States
- Southeast Retina Center, Augusta, Georgia, United States
- Georgia Retina, P.C., Marietta, Georgia, 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.
Open NCT04603937 on ClinicalTrials.govOther trials for Central retinal vein occlusion
Additional recruiting or active studies for the same condition.
- ENROLLING BY INVITATIONPHASE4NCT07456826Study Evaluating the Efficacy and Safety of Chloroprocaine HCl Ophthalmic Gel 3% vs Proparacaine Ophthalmic Solution 0.5% Plus Subconjunctival Lidocaine in Patients Undergoing Intravitreal InjectionsHarrow Inc
- ENROLLING BY INVITATIONNANCT07318428AI-Assisted Detection of Posterior Segment Diseases: DR, AMD, RVO, and GlaucomaInje University
- RECRUITINGNCT07308639DATA-INSIGHT is a Project That Looks at Health Data in Germany to Find Out How Many Patients Suffer From Eye Disease. The Project Also Explores New Ways to Collect and Use Publicly Available Healthcare Information.Bayer
- RECRUITINGPHASE2NCT07259928Safety and Proof of Concept Study of ANXV (Annexin A5) in Patients With Diabetic Retinopathy or Retinal Vein OcclusionAnnexin Pharmaceuticals AB
- RECRUITINGEARLY PHASE1NCT04008121Feasibility and Safety of MB-102 in Ocular Angiography as Compared to Fluorescein SodiumMediBeacon
- RECRUITINGNCT07550777Serum Cholinesterases, Paraoxonase, and Cardiovascular Risk After Intravitreal BevacizumabAtaturk University
- RECRUITINGPHASE2NCT07205887A Dose-masked Study of Intravitreal EYE103 in Participants With NVAMD or Macular Edema Following BRVOEyeBiotech Ltd.
- RECRUITINGNANCT07002372Effect of Video Viewing on Intravitreal Injection ExperienceSecond Affiliated Hospital, School of Medicine, Zhejiang University