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Terminated Phase 1 Interventional

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

ClinicalTrials.gov ID: NCT03790852

Public ClinicalTrials.gov record NCT03790852. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Sep 3, 2026, 1:00 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Phase 1/1b Open Label, Multi-center 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 Wet Age-Related Macular Degeneration (wAMD), Diabetic Macular Edema (DME) and Retinal Vein Occlusion (RVO)

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

This is a Phase 1b open-label study to assess the bioactivity, ocular and systemic safety, tolerability, and pharmacokinetics of repeated injections of KSI-301 at two dose levels: 2.5 mg and 5 mg

Study identification

NCT ID
NCT03790852
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 1
Lead sponsor
Kodiak Sciences Inc
Industry
Enrollment
121 participants

Conditions and interventions

Eligibility (public fields only)

Age range
21 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Dec 25, 2018
Primary completion
Jun 1, 2021
Completion
Jun 8, 2022
Last update posted
Mar 19, 2024

2018 – 2022

United States locations

U.S. sites
11
U.S. states
6
U.S. cities
11
Facility City State ZIP Site status
Retinal Research Institute, LLC Phoenix Arizona 85053
Retina Vitreous Associates Medical Group Beverly Hills California 90211
Northern California Retina Vitreous Associates Mountain View California 94040
Byers Eye Institute at Stanford Palo Alto California 94303
Retina Vitreous Associates of Florida St. Petersburg Florida 33711
Sierra Eye Associates Reno Nevada 89502
Mid Atlantic Retina Philadelphia Pennsylvania 19107
Retina Research Institute of Texas Abilene Texas 79606
Austin Clinical Research Austin Texas 78750
Retina Consultants of Texas Bellaire Texas 77401
Retina Consultants of Texas Woodlands The Woodlands Texas 77384

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

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About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT03790852, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Mar 19, 2024 · Synced Sep 3, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT03790852 live on ClinicalTrials.gov.

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