Last updated on October 2017

Efficacy and Safety of Two Different Aflibercept Regimens in Subjects With Neovascular Age-related Macular Degeneration (nAMD)


Brief description of study

To compare the efficacy of 2 mg aflibercept administered by two different intravitreal (IVT) treatment regimens to subjects with neovascular age-related macular degeneration (nAMD)

Detailed Study Description

330 Patients who have completed at least one year of treatment with aflibercept will be randomized to two different aflibercept regimens and followed for 76 weeks.

Clinical Study Identifier: NCT02540954

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Bayer Clinical Trials Contact

Clinique medicale de l'oeil de l'Estrie
Sherbrooke, QC Canada
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L'Hospitalet de Llobregat, Spain
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Southampton, United Kingdom
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Great Yarmouth, United Kingdom
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Newcastle Upon Tyne, United Kingdom
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