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argenxglobal

We’re the immunology innovation company, advancing understanding and possibilities for people living with diseases that have been underserved.

We challenge conventions and pursue bold pathways with one goal: progress for the people who need it now.

10/30/2026

The search for answers doesn’t always have the same beginning.

Early signs of autoimmune diseases can take many forms. What begins as an initial unfamiliar change can lead to a journey toward understanding the symptoms being experienced.

While each person’s path to diagnosis varies, receiving those answers can be a pivotal moment that provides a great sense of clarity.

Hear more in the full episode of The Unseen Story, our series exploring the unseen realities of life with an autoimmune condition: https://bit.ly/4Bz8PqB

10/27/2026

Sandy received her myasthenia gravis (MG) diagnosis at age 60. As her symptoms began affecting her ability to work, she eventually retired earlier than she had planned.

Now, Sandy stays connected to her family, friends and local MG community. She also helps organize a face-to-face support group where people living with MG can exchange experiences, learn from one another and spend time with people who understand the condition.

Research shows that MG frequently develops later in life, making awareness of the condition among older adults especially important.

Learn more about aging with MG and listen to Sandy's experience on Untold Stories: Life with a Severe Autoimmune Condition: https://bit.ly/4sL6oNP

10/16/2026

What can you expect when taking part in a clinical trial?

From screening to ongoing care and support, each part of a clinical trial is designed with participants’ safety and well-being in mind.

Watch to learn about three important parts of the clinical trial experience and how participants are supported along the way.

Learn more about clinical research and explore argenx clinical trials: https://bit.ly/4ylDq83

10/13/2026

After waiting nearly six years for an MG diagnosis, Lea found a community that understood her experience.

She used social media to find connection with others in Germany, and beyond, living with . Together, they exchange experiences, share what helps them navigate life with MG, and create a space where Lea feels understood.

Lea’s story shows that, while experiences with diagnosis and care may differ across countries and healthcare systems, connection can reach beyond geographic borders.

Hear more from Lea on Untold Stories: Life with a Severe Autoimmune Condition: https://bit.ly/4hMuVOs

10/06/2026

Entrepreneurial Science shapes how we work.

We believe innovation happens when academic discovery, clinical insight and patient experience come together.

For people living with complex diseases and those who support them, progress is personal. We listen to patient perspectives to help guide our objectives and pursue better answers.

Today, we’re bringing that same spirit forward in how we show up as argenx.

See how Entrepreneurial Science comes to life at argenx: https://bit.ly/3TMmhGy

10/05/2026

If you or someone you care about is considering a clinical research study, talking with your healthcare provider is a great place to start. They can help answer your questions, discuss your options, and support you in making an informed decision.

Swipe to read some ways HCPs can help in the decision-making process.

09/30/2026

Deciding whether to join a clinical research study is a personal choice, and there is no right or wrong answer. Take the time to gather the information you need to make a decision that feels right for you.

In this post, you’ll find a few questions to ask yourself as you consider your options.

09/23/2026

Muscular dystrophy isn’t one disease, and there isn’t one way to experience it.

More than 30 genetic diseases fall under the muscular dystrophy umbrella. Some begin in childhood, while others may not appear until adulthood. Different forms can affect different muscles and progress at different rates.

Whether you’re living with muscular dystrophy or supporting someone who is, understanding those differences can help explain why experiences can look so different from person to person.

This September, we’re proud to support our partner, the Muscular Dystrophy Association (MDA), and its campaign. See what inspires Cristian when he thinks about the MDA community.

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33 Arch Street, 32nd Floor Suite 3201
Boston, MA

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https://www.argenx.com/

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