retinal vein occlusion

Innovative biologic prefilled syringe approved in EU

13 December 2024 | By Catherine Eckford (European Pharmaceutical Review)

The new treatment option provides a convenient alternative to currently available vials of the bispecific antibody for EU patients with common vision conditions.

news

Sandoz to file for approval of aflibercept biosimilar

16 August 2023 | By Caroline Peachey (European Pharmaceutical Review)

Sandoz intends to seek regulatory approval for its aflibercept biosimilar in the US and EU in the coming months.

news

MHRA approves biosimilar for vision disorders in Great Britain

17 January 2023 | By Catherine Eckford (European Pharmaceutical Review)

A marketing authorization for Ximluci® biosimilar referencing Lucentis® (ranibizumab) in Great Britain has been issued by the Medicines and Healthcare products Regulatory Agency (MHRA).

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retinal vein occlusion

Innovative biologic prefilled syringe approved in EU

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