Dupixent is indicated to treat severe atopic dermatitis in children aged six months to five years. Credit: Luma Pimentel on Unsplash.

Sanofi has secured approval for Dupixent (dupilumab) from the European Commission (EC) to treat severe atopic dermatitis in children aged six months to five years, who are systemic therapy candidates, in the European Union (EU).

This approval makes Dupixent the first and only medicine available in the US and Europe for the treatment of such young children.

Go deeper with GlobalData

Data Insights

The gold standard of business intelligence.

Find out more

Related Company Profiles

View all

Dupixent is a fully human monoclonal antibody which blocks the signalling of interleukin-4 (IL-4) and interleukin-13 (IL-13) pathways.

It has received regulatory approval in many countries for the treatment of chronic rhinosinusitis with nasal polyposis (CRSwNP), asthma, eosinophilic esophagitis (EoE) and prurigo nodularis in different age groups.

Head of Sanofi Immunology and Inflammation Global Development, Naimish Patel, said: “The vast majority of people with atopic dermatitis begin to develop symptoms during their earliest, most vulnerable years, and these symptoms can often continue throughout their lives.

“With this latest approval, Dupixent is the first-ever biologic medicine for people living with atopic dermatitis from infancy to adulthood.

How well do you really know your competitors?

Access the most comprehensive Company Profiles on the market, powered by GlobalData. Save hours of research. Gain competitive edge.

Company Profile – free sample

Thank you!

Your download email will arrive shortly

Not ready to buy yet? Download a free sample

We are confident about the unique quality of our Company Profiles. However, we want you to make the most beneficial decision for your business, so we offer a free sample that you can download by submitting the below form

By GlobalData
Visit our Privacy Policy for more information about our services, how we may use, process and share your personal data, including information of your rights in respect of your personal data and how you can unsubscribe from future marketing communications. Our services are intended for corporate subscribers and you warrant that the email address submitted is your corporate email address.

“Given its well-established safety and efficacy profile, Dupixent has the potential to transform the landscape for people of all ages living with atopic dermatitis.”

The regulatory approval is based on the data obtained from a Phase III trial.

The placebo-controlled, randomised, double-blind trial assessed the safety and efficacy of Dupixent along with standard of care low-potency topical corticosteroids (TCS) compared to low-potency TCS alone (placebo) in 162 moderate to severe atopic dermatitis patients aged six months to five years.

Dupixent was found to improve skin clearance and reduce overall disease severity and itch compared to a placebo.

In the overall disease population and among those severely affected, the antibody also improved skin pain, sleep quality and quality of life compared to a placebo.