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Study identifier: NCT07389980 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

Prospective Trial of the Efficacy and Safety of a Personalized Regimen of High-dose Aflibercept 8mg on Treatment-naive Polypoidal Choroidal Vasculopathy: the PALLAS Trial

Condition: Polypoidal Choroidal Vasculopathy · Polypoidal Choroidal Vasculopathy (PCV)  ·  Sponsor: Yeungnam University College of Medicine

PhasePhase 3
Planned participants50
Who can joinAll sexes, 19 Years to no upper limit
Healthy volunteersNo

About this study

The purpose of this study is to evaluate the efficacy and safety of the aflibercept 8 mg used in a personalized regimen, with flexible loading dose and treatment intervals from 8 to 24 weeks in eyes with treatment-naive PCV.

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

Talk to the study team

Sohee Shin  ·  82-53-620-3440  ·  ey005@ymc.yu.ac.kr

Always discuss trial participation with your own doctor first.

Locations (1)

Yeungnam University HospitalDaegu, South KoreaRecruiting

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Source record: clinicaltrials.gov/study/NCT07389980