argenxglobal

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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.

10/16/2026

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

If you or someone you care about is considering a clinical research study, talking with your healthcare provider is a gr...
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.

Deciding whether to join a clinical research study is a personal choice, and there is no right or wrong answer. Take the...
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.

Muscular dystrophy isn’t one disease, and there isn’t one way to experience it. ​​More than 30 genetic diseases fall und...
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.​

09/22/2026

When you live with multiple autoimmune conditions, recognizing new symptoms isn't always straightforward.​

Jasmine had already been managing lupus, rheumatoid arthritis and Raynaud's syndrome for years when she began noticing numbness in her hands and feet that felt different. ​

That change led her to continue asking questions, ultimately resulting in a diagnosis of chronic inflammatory demyelinating polyneuropathy (CIDP).​

Her story highlights one of the challenges many people with chronic illness face: it can take time to understand what's changing when symptoms overlap. ​

During , Jasmine’s experience reminds us that noting changes and discussing them as early as possible with your healthcare team is an important part of navigating life with chronic illness.​

Listen to the episode of Untold Stories: Life with a Severe Autoimmune Condition: https://bit.ly/46CnZx2​

09/21/2026

Sometimes the first signs of myositis appear in the everyday movements we take for granted.​

🙋 Reaching overhead​
🪑 Standing up from a chair​
🪜 Climbing stairs​​

These routine movements can gradually become more difficult as muscle weakness progresses – often long before others recognize what’s happening.​

This , we’re highlighting the everyday impact of myositis and why recognizing these often-overlooked changes is an important step toward earlier recognition. Explore more: https://bit.ly/4he5eEV​

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