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

PHASE1TerminatedINTERVENTIONAL
Enrollment

121

Participants

Timeline

Start Date

December 26, 2018

Primary Completion Date

June 2, 2021

Study Completion Date

June 9, 2022

Conditions
Wet Age-related Macular DegenerationRetinal Vein OcclusionDiabetic Macular Edema
Interventions
DRUG

KSI-301

Intravitreal injection

Trial Locations (11)

19107

Mid Atlantic Retina, Philadelphia

33711

Retina Vitreous Associates of Florida, St. Petersburg

77384

Retina Consultants of Texas Woodlands, The Woodlands

77401

Retina Consultants of Texas, Bellaire

78750

Austin Clinical Research, Austin

79606

Retina Research Institute of Texas, Abilene

85053

Retinal Research Institute, LLC, Phoenix

89502

Sierra Eye Associates, Reno

90211

Retina Vitreous Associates Medical Group, Beverly Hills

94040

Northern California Retina Vitreous Associates, Mountain View

94303

Byers Eye Institute at Stanford, Palo Alto

Sponsors
All Listed Sponsors
lead

Kodiak Sciences Inc

INDUSTRY

NCT03790852 - 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 | Biotech Hunter | Biotech Hunter