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Study identifier: NCT07425522 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

A Study to Evaluate the Safety, Tolerability, Pharmacodynamics, and Pharmacokinetics of RO7823653 in Participants With Diabetic Macular Edema (DME)

Condition: Diabetic Macular Edema  ·  Sponsor: Genentech, Inc.

PhasePhase 1
Planned participants93
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

The purpose of this study is to evaluate the safety, tolerability, Pharmacodynamics (PD), and Pharmacokinetics (PK) of multiple doses of RO7823653 in participants with DME, administered by intravitreal (IVT) injection as monotherapy and co-administered with faricimab.

This description comes directly from the study's public registry record.

Talk to the study team

Reference Study ID Number GR46431 https://forpatients.roche.com/ No attachments to email below.  ·  888-662-6728 (U.S. and Canada)  ·  global-roche-genentech-trials@gene.com

Fastest response: use the inquiry form. https://www.gene.com/contact-us/submit-medical-inquiry

Always discuss trial participation with your own doctor first.

Locations (10)

Associated Retina Consultants - Peoria - DocTrials - PPDSPeoria, Arizona, United StatesRecruiting
Retina-Vitreous Associates Medical GroupBeverly Hills, California, United StatesRecruiting
Bay Area Retina Specialists Medical Group - Vestrum - PPDSWalnut Creek, California, United StatesRecruiting
Retina Vitreous Associates of FloridaSt. Petersburg, Florida, United StatesRecruiting
Erie Retina Research, LLC - 300 State StErie, Pennsylvania, United StatesRecruiting
Charles Retina InstituteGermantown, Tennessee, United StatesRecruiting
Retina Research Institute of TexasAbilene, Texas, United StatesRecruiting
Austin Clinical Research, LLCAustin, Texas, United StatesRecruiting
Retina Consultants of Texas Westover Hills Retina CenterSan Antonio, Texas, United StatesRecruiting
Piedmont Eye CenterLynchburg, Virginia, United StatesRecruiting

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Source record: clinicaltrials.gov/study/NCT07425522