This study is conducted to evaluate the safety of a single intravitreal injection of THR-687.
Study Type
INTERVENTIONAL
Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
12
single intravitreal injection of THR-687 dose level 1
single intravitreal injection of THR-687 dose level 2
single intravitreal injection of THR-687 dose level 3
Retina Consultants of Arizona
Phoenix, Arizona, United States
Center for Retina and Macular Disease
Winter Haven, Florida, United States
Midwest Eye Institute
Indianapolis, Indiana, United States
Sierra Eye Associates
Reno, Nevada, United States
Incidence of dose-limiting toxicities up to the Day 14 visit
Time frame: From Day 0 up to Day 14
Incidence of systemic and ocular adverse events including serious adverse events up to the end of the study
Time frame: From Day 0 up to Day 84
Occurrence of laboratory abnormalities up to the end of the study
Time frame: At Screening, Day 1, Day 7, Day 28 and Day 84
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Palmetto Retinal Center
West Columbia, South Carolina, United States
Retina Research Institute of Texas
Abilene, Texas, United States
Valley Retina Institute, PA
McAllen, Texas, United States