Active, not recruitingPhase 1NCT06847854
A Study to Investigate the Safety, Tolerability, Pharmacokinetics (PK) and Pharmacodynamics (PD) of RO7497372 in Participants With Diabetic Macular Edema (DME)
Studying Central retinal vein occlusion
Last synced from ClinicalTrials.gov
ℹ
Clinical trial records are synced from ClinicalTrials.gov through automated extraction.
Report missing dataKey facts
- Sponsor
- Genentech, Inc.
- Principal Investigator
- Clinical TrialsHoffmann-La Roche
- Intervention
- RO7497372(drug)
- Enrollment
- 151 target
- Eligibility
- 18 years · All sexes
- Timeline
- 2022 – 2027
Study locations (30)
- Barnet Dulaney Perkins Eye Center, Mesa, Arizona, United States
- Retinal Consultants of AZ, Ltd, Peoria, Arizona, United States
- Associated Retina Consultants, Phoenix, Arizona, United States
- Arkansas Retina Research, Little Rock, Arkansas, United States
- Global Research Management, Glendale, California, United States
- Retinal Consultants Medical Group, Modesto, California, United States
- Bay Area Retina Associates, Walnut Creek, California, United States
- Florida Eye Associates, Melbourne, Florida, United States
- Medeye Associates, Miami, Florida, United States
- East Florida Eye Institute, Stuart, Florida, United States
- Retina Specialists of Tampa, Wesley Chapel, Florida, United States
- Center for Retina and Macula Disease, Winter Haven, Florida, United States
- Cumberland Valley Retina PC, Hagerstown, Maryland, United States
- Retina Associates of Michigan, Grand Blanc, Michigan, United States
- Foundation for Vision Research, Grand Rapids, Michigan, United States
- +15 more locations on ClinicalTrials.gov
Primary source
Recruitment status, site addresses, contacts, and full eligibility criteria can change between syncs. Always verify with the trial team before planning travel or treatment.
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