This study will assess the safety, tolerability, and pharmacokinetics (PK) of intravitreal (IVT) injections of RO7663498 in participants with diabetic retinopathy (DR).
Study Type
INTERVENTIONAL
Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
30
Participants will receive RO7663498 as per the schedule defined in the protocol.
Global Research Management
Glendale, California, United States
RECRUITINGUniversity Retina and Macula Associates, PC
Oak Forest, Illinois, United States
RECRUITINGOhio State Havener Eye Institute;Ophthalmology Research
Columbus, Ohio, United States
RECRUITINGPercentage of Participants With Ocular Adverse Events (AEs)
Time frame: Up to Week 20
Percentage of Participants With Systemic (non-ocular) AEs
Time frame: Up to Week 20
Number of Abnormalities Recorded in Standard Ophthalmological Assessments
Time frame: Up to Week 20
Aqueous Humor (AH) Concentrations of RO7663498
Time frame: Up to Week 12
Serum Concentrations of RO7663498
Time frame: Up to Week 20
Reference Study ID Number: BP46156 https://forpatients.roche.com/ No email attachments.
CONTACT
Fastest response: use the inquiry form. https://www.gene.com/contact-us/submit-medical-inquiry
CONTACT
This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.