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Aflibercept 8 mg approved for retinal vein occlusion (RVO) in the UK.
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Suitable for treating visual impairment from RVO.
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Approval based on QUASAR trial data.
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8 mg group had fewer injections and similar visual outcomes as 2 mg.
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Over 60% of patients in 8 mg achieved longer treatment intervals.
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Safety profile consistent with previous studies.
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Updated posology allows minimum 4-week treatment intervals.
Original Source(s)
UK Authorization for Aflibercept
MHRA clears Eylea for macular edema following retinal vein occlusion
March 3, 2026
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