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Novartis reports one year results of phase III MERLIN study evaluating Beovu every four week dosing and provides update on Beovu clinical program..

Read time: 1 mins
Last updated:30th Jul 2021
Published:30th May 2021
Novartis reported the first interpretable year one results of the Phase III MERLIN study, a two-year study initiated in H2 2018, assessing the efficacy and safety of Beovu (brolucizumab) 6 mg versus aflibercept 2 mg given every four weeks following the loading phase in patients with wet age-related macular degeneration (AMD) who have persistent retinal fluid despite anti-VEGF therapy.
Condition: Age Related Macular Degeneration
Type: drug
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