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argenx

@argenxglobal

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Driven by curiosity and the people who need progress now. We’re the immunology innovation company pursuing bold pathways to expand possibilities.

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Entrepreneurial Science shapes how we work.

It starts with bringing different perspectives together, from patient experience to clinical insight and academic discovery, and learning from each other through co-creation.

For us, that means pursuing bold pathways and working to move immunology science faster than thought possible for patients who need progress now.

And as argenx continues to evolve, we’re bringing that same spirit forward in how we show up.

Visit the link in our bio to see how Entrepreneurial Science comes to life at argenx.

#EntrepreneurialScience by @argenxglobal

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13 days ago

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 by clicking the link in our bio.

#ClinicalResearch #ClinicalTrials #AutoimmuneDisease #Research #argenx by @argenxglobal

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3 days ago

Lea turned to social media after her MG diagnosis to connect with those in Germany, and beyond, living with #MyastheniaGravis.

The result was new-found community for exchanging experiences, sharing tips for navigating MG, and creating a space to feel understood.

Hear how Lea finds connection across borders on Untold Stories: Life with a Severe Autoimmune Condition at the link in bio. by @argenxglobal

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6 days ago

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. by @argenxglobal

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14 days ago

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. by @argenxglobal

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19 days ago

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 #MDAstrong campaign. See what the MDA community means to Cristian.

#TogetherWeDiscover by @argenxglobal

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a month ago

Living with autoimmune conditions can make it difficult to recognize when something new is happening.

That's why Jasmine spent years assuming numbness was from managing lupus, rheumatoid arthritis and Raynaud's syndrome before realizing it was more pronounced. That observation eventually led to a new diagnosis of CIDP.

Recognizing change isn't always easy—especially when symptoms can overlap.

This #RheumatoidAwarenessMonth, Jasmine’s journey is a reminder that paying attention to changes and talking with your healthcare team about new or worsening symptoms is an important part of understanding your health.

Listen to her story on Untold Stories: Life with a Severe Autoimmune Condition podcast at the link in bio.

#TogetherWeDiscover by @argenxglobal

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a month ago

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.

On #WorldMyositisDay and every day, we recognize the impact of myositis and why greater understanding of these often-overlooked changes is an important step toward earlier recognition.

#TogetherWeDiscover by @argenxglobal

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a month ago

A platelet count measures platelets – the blood cells that help stop bleeding – not the full impact of living with ITP.

Some of the most challenging aspects of living with immune thrombocytopenia (ITP) – fatigue, brain fog, anxiety, and uncertainty – aren’t reflected in a lab result.

This #ITPAwarenessMonth, explore beyond the data as we shine a light on parts of living with ITP that can’t be measured by a lab test.

#TogetherWeDiscover by @argenxglobal

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a month ago

If you’re considering participating in clinical research, learning what to expect can help you feel more informed and prepared.

Follow these key steps to better understand what the process may look like. by @argenxglobal

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a month ago

Finding connection doesn’t always mean expanding your circle—it can mean finding people who understand your experience in a way others can’t.

Morgan shares her story of how connecting with the myathenia gravis (MG) community helped her feel less alone and gave her the confidence to tell her story on her own terms.

Listen now to Untold Stories: Life with a Severe Autoimmune Condition at the link in bio.

#TogetherWeDiscover by @argenxglobal

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a month ago

Living with an autoimmune rheumatic disease can mean carrying more than meets the eye.

What’s happening inside the body isn’t always reflected by what others can see on the outside. This #RheumaticDiseaseAwarenessMonth, we’re helping connect what’s happening beneath the surface with the realities of living with these conditions.

Share this post to help others see beyond what’s visible.

#TogetherWeDiscover by @argenxglobal

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2 months ago