Mark Barakat, MD: Stable IOP Outcomes After Aflibercept 8 mg in DME
Pre-dose IOP outcomes in eyes with DME receiving intravitreal aflibercept 8 mg or 2 mg were comparable and remained stable through Week 48.
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Pre-dose IOP outcomes in eyes with DME receiving intravitreal aflibercept 8 mg or 2 mg were comparable and remained stable through Week 48.
VenoStent Enrolls First Subjects in 200-Subject US Clinical Trial
First-year results from ALTITUDE suggest RGX-314 was well-tolerated and provided meaningful improvements in disease severity at dose levels 1 and 2.
ABBV-RGX-314 continues to be well tolerated in 50 patients from dose levels 1 and 2 (Cohorts 1-3) with no drug-related serious adverse events Dose level 2...
Mark Barakat, MD, reviews the best practices for patient communication and shared decision making.