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Dupixent Receives 2025 Prix Galien USA Award for Innovation

Dupixent Receives 2025 Prix Galien USA Award for Innovation

Dupixent Achieves Recognition at 2025 Prix Galien USA Awards

In a notable achievement for Regeneron Pharmaceuticals, Dupixent (dupilumab) has been awarded the title of “Best Biotechnology Product” for 2025 by the prestigious Galien Foundation. This accolade celebrates significant advancements in medical science, particularly in therapies that transform patient care.

Groundbreaking Innovation in Biotechnology

Dupixent stands out as the first and only medication targeting the IL-4 and IL-13 signaling pathways, which are crucial in the process of type 2 inflammation associated with various allergic and atopic conditions. The award was presented during a ceremony in New York City, marking it as the second time Regeneron has earned this honor, following the recognition of Inmazeb (atoltivimab, maftivimab, and odesivimab-ebgn) in 2022.

Statements from Regeneron Leadership

George D. Yancopoulos, M.D., Ph.D., President and Chief Scientific Officer at Regeneron, expressed pride in this recognition. He noted that Dupixent exemplifies a ‘first-in-class’ breakthrough therapy, providing treatment for an array of serious conditions that were previously challenging to manage. With more than one million patients receiving treatment globally, the impact of Dupixent is profound, as it aims to alleviate various allergic and atopic diseases sharing the same inflammatory mechanisms.

Clinical Validation of Dupixent

Dupixent was developed based on a comprehensive scientific hypothesis, predicting that many allergic diseases are driven by the overactivity of interleukin-4 (IL-4) and interleukin-13 (IL-13). The results from Phase 3 trials have showcased substantial clinical benefits across multiple allergic conditions, further reinforcing this hypothesis.

Latest Approvals and Indications

Globally, Dupixent is approved for eight distinct conditions, stretching from rare diseases to more common ailments. Among its latest approvals is the 2024 designation by the U.S. Food and Drug Administration (FDA) as an additional maintenance treatment for adults battling inadequately controlled chronic obstructive pulmonary disease (COPD) with an eosinophilic phenotype.

Patient Safety and Side Effects

As with any medication, Dupixent may cause side effects. The most commonly reported issues include injection site reactions, respiratory infections, and visual disturbances. While important, it is crucial for patients to discuss any adverse reactions with their healthcare providers to ensure optimal treatment.

About Dupixent

Utilizing Regeneron’s proprietary VelocImmune technology, Dupixent is a fully human monoclonal antibody that operates without effecting immunosuppression. This unique formulation is instrumental in reducing type 2 inflammation, contributing to successful management of several diseases through clinical trials.

Ongoing Development of Dupilumab

Dupilumab’s journey is supported by Regeneron and Sanofi through a collaborative global agreement. Ongoing studies are currently examining this therapy across various diseases characterized by type 2 inflammation beyond those already approved, highlighting its potential for expanded applications.

U.S. Indications for Dupixent

In the United States, Dupixent is indicated for the treatment of multiple conditions, including:

  • Moderate-to-severe eczema (atopic dermatitis).
  • Severe asthma, particularly eosinophilic or oral steroid-dependent asthma.
  • Chronic rhinosinusitis with nasal polyps.
  • Eosinophilic esophagitis.
  • Prurigo nodularis.
  • Chronic obstructive pulmonary disease.
  • Chronic spontaneous urticaria.
  • Bullous pemphigoid.

It is vital to note that Dupixent does not serve as a rescue medication for sudden asthma or allergic reactions.

Important Safety Information

Patients are advised to consult their healthcare provider before starting Dupixent, particularly if they have a history of eye disorders or other medical conditions. Potential allergic reactions may occur, and immediate medical attention is necessary if severe symptoms arise.

Contacts and Additional Information

For more inquiries regarding Dupixent or Regeneron’s products, please contact:

Media Relations: Daren Kwok, Tel: +1 914-847-1328, Email: Daren.Kwok@regeneron.com

Investor Relations: Mark Hudson, Tel: +1 914-847-3482, Email: Mark.Hudson@regeneron.com

Frequently Asked Questions

What is Dupixent used for?

Dupixent is prescribed for treating several allergic and atopic conditions, including asthma, eczema, and chronic rhinosinusitis.

What is the active ingredient in Dupixent?

The active ingredient in Dupixent is dupilumab, which inhibits IL-4 and IL-13 signaling pathways.

Who can take Dupixent?

Dupixent is approved for use in patients aged 6 months and older, depending on the specific condition being treated.

Are there any common side effects of Dupixent?

Common side effects include injection site reactions, respiratory infections, and potential eye-related issues.

Where can I find more information about Dupixent?

For detailed information, you may contact Regeneron or visit their official website.

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