TerminatedPhase 1NCT03790852
Exploratory Study to Investigate the Bioactivity, Ocular and Systemic Safety, Tolerability, and Pharmacokinetics Following Single and Multiple Intravitreal Administrations of KSI-301 in Subjects With wAMD, DME and 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
- 121 enrolled
- Eligibility
- 21 years · All sexes
- Timeline
- 2018 – 2022
Study locations (11)
- Retinal Research Institute, LLC, Phoenix, Arizona, United States
- Retina Vitreous Associates Medical Group, Beverly Hills, California, United States
- Northern California Retina Vitreous Associates, Mountain View, California, United States
- Byers Eye Institute at Stanford, Palo Alto, California, United States
- Retina Vitreous Associates of Florida, St. Petersburg, Florida, United States
- Sierra Eye Associates, Reno, Nevada, United States
- Mid Atlantic Retina, Philadelphia, Pennsylvania, United States
- Retina Research Institute of Texas, Abilene, Texas, United States
- Austin Clinical Research, Austin, Texas, United States
- Retina Consultants of Texas, Bellaire, Texas, United States
- Retina Consultants of Texas Woodlands, The Woodlands, Texas, United States
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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