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MHRA approves low-dose atropine eye drops for slowing myopia progression

Ryjunea, a 0.1 mg/ml atropine eye drop, has been cleared by the Medicines and Healthcare products Regulatory Agency for use in myopia control

A woman instills an eye drop in the eye of a boy
Getty/Tom Le Goff

The Medicines and Healthcare products Regulatory Agency (MHRA) has approved Ryjunea for slowing myopia progression.

It is the first time the MHRA has approved a low-dose atropine eye drop for myopia control.

Ryjunea has been cleared for use in children aged between three and 14, with a progression rate of 0.5 D or more per year and a severity of -0.5 D to -6.0 D.

The MHRA approval follows authorisation of Ryjunea by the European Commission for myopia control in June.

Professor Annegret Dahlmann-Noor, a consultant ophthalmologist at Moorfields Eye Hospital, highlighted that childhood myopia increases the risk of eye disease later in life.

“We have a critical window in childhood to recognise myopia and act early,” she said.

“A comprehensive approach, combining lifestyle habits, optical correction, and approved medical options, gives children the best chance to support healthy vision into adulthood,” she emphasised.

Neil Parkin, UK & Ireland general manager for Ryjunea manufacturer, Santen, described the MHRA approval as an “important milestone” in improving awareness and access to care among children with myopia.

“We want to help shift the conversation from correction to control, supporting clinicians, schools, and parents to take early action,” he said.

The National Institute for Health and Clinical Excellence is currently investigating the cost-effectiveness and clinical efficacy of low-dose atropine eye drops for managing myopia among young people between the ages of three and 14.

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