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Long-term efficacy and safety of Eylea 8 mg (aflibercept 8 mg) with extended dosing intervals in wet age-related macular degeneration confirmed at three years – Bayer

Written by | 29 Jul 2025

Bayer and its collaboration partner Regeneron presented results from the open-label extension study of the clinical trial PULSAR in patients with neovascular (wet) age-related macular degeneration (nAMD) at… read more.

Eylea (aflibercept) 8 mg approved in China for wet age-related macular degeneration – Bayer

Written by | 9 Jul 2025

The Center for Drug Evaluation (CDE) of China’s National Medical Products Administration (NMPA) has approved Eylea 8 mg (aflibercept 8 mg) for the treatment of neovascular (wet) age-related… read more.

Eylea (aflibercept) 8 mg with extended 6-month treatment interval recommended for approval in EU – Bayer

Written by | 29 May 2025

Bayer announced that the Committee for Medicinal Products for Human Use (CHMP) of the EMA has issued a positive opinion recommending a label extension for Eylea 8 mg… read more.

Long-term efficacy and safety profile of Eylea 8 mg with extended dosing intervals in diabetic macular edema confirmed at three years – Bayer

Written by | 28 Oct 2024

Bayer and its collaboration partner Regeneron presented results from the open-label extension study of the clinical trial PHOTON in patients with diabetic macular edema (DME) at three years,… read more.

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