UCB USA

UCB USA Official U.S. page for UCB Biopharma. Patients are at the heart of everything we do. Learn more at www.ucb-usa.com.

UCB is a global biopharmaceutical company focused on creating value for people living with severe diseases in immunology and neurology. We are unwavering in our purpose: delivering moments that matter for people impacted by severe diseases, now and into the future. People are at the heart of everything we do, inspiring us, driving our scientific discovery, and leading us to rethink the patient experience. We work with stakeholders to address the unmet needs of patients and caregivers, helping them to achieve their goals and to live the lives they want. UCB is on a journey to be the patient-preferred biopharma leader by delivering medicines and solutions that improve lives while creating value for society.

10/15/2025

Let’s work together to raise awareness of SUDEP: Sudden Unexpected Death in Epilepsy. 💜​

Through partnerships with advocacy organizations, we’ve co-created a Clinical Toolkit for Preventing Epilepsy Deaths, designed to equip healthcare providers, patients, and caregivers with resources to understand and reduce risk, which you can find at https://bit.ly/3JFF9zz

10/14/2025

Nearly 3.5 million people in the U.S. live with epilepsy, yet many face barriers to care, including limited access to specialists, mental health support and even transportation. ​

We’re taking action to help break down these barriers through our new community health worker initiative, an innovative partnership with Morehouse School of Medicine we believe will enhance healthcare for epilepsy patients in Georgia through community-based care pathways. ​

Learn more and discover how collaboration can help elevate lives: https://bit.ly/3W5rI0Q

10/11/2025

Reaching as many people as possible starts with clear communication, which is why it’s so important to provide support in a variety of languages. Our Spanish-speaking resources, like C.A.R.E Binder and our partnership with Tu Salud Tu Familia, were specifically developed to reduce these barriers by giving everyone better access to tools that can truly make a difference. 💙 ​

10/10/2025

Travel is always exciting, but it can be overwhelming, especially for people living with epilepsy. But here's the thing: preparation can make all the difference! 💜​

We've spent more than 30 years working alongside the epilepsy community to understand the challenges they face and make resources to help them live more confidently, whether at home or across the world. ​

These practical tips for traveling with epilepsy can help make your next trip safer, smoother and nothing short of amazing.

10/08/2025

From a Guinness World Records record-breaking ball of bandages to a powerful runway show, Times Square became a stage for HS awareness.​

We’re proud to have stood alongside HS Connect - Hidradenitis Suppurativa Connect, Make HStory and so many HS warriors in this historic moment that truly reaffirms our commitment to advocacy, innovation, and overall care for the HS community. 💙

10/07/2025

Awareness is the first step toward diagnosis. For people living with rare diseases like Myasthenia Gravis (MG), Spanish-language resources are limited, yet they can make all the difference in helping patients and families feel informed and supported.​

That's why we’ve partnered with Spanish-language program Tu Salud Tu Familia to sponsor a series explaining Myasthenia Gravis, featuring conversations with both patients and healthcare providers. ​

Learn more by watching the full episode and explore more from the series via https://bit.ly/46FNAG9 🎥

10/04/2025

We’re in Times Square today with to celebrate the strength and resilience of the HS (Hidradenitis Suppurativa) community. 💜💙Together we broke the with the world’s largest ball of bandages, symbolizing the countless bandages people with HS use every day. We’re honored to stand alongside to raise awareness in NYC! ✨

09/26/2025

Behind every advance in rare epilepsy care is a simple truth: progress starts with listening. 💙​

As Brad Chapman, Head of U.S. Epilepsy & Rare Syndromes, explains, our partnerships with families living with Lennox-Gastaut Syndrome (LGS) and Dravet syndrome (DS) guide how we push the science forward, from today’s solutions to tomorrow’s breakthroughs.​

When science and community come together, real change becomes possible. ​Learn more at https://bit.ly/4mxzoUf

09/19/2025

The most meaningful moments in science often come after years of persistence — those rare “aha” discoveries 💡 where the data shows real potential for a breakthrough that could elevate patient lives.​

It’s those moments that fuel our research team, turning challenges into hope and science into solutions. 💙 Learn more about UCB’s journey to advance science and deliver meaningful innovations for patients https://bit.ly/4k6W7X0

09/18/2025

When you live with HS (hidradenitis suppurativa) or PsA (psoriatic arthritis), pain is always part of the picture, yet it often seems invisible to others. Chronic pain can be a daily struggle that makes normal routines feel out of reach.​

💙Our partnership with these communities goes beyond the solutions we’ve developed. We’re focused on helping elevate lives by listening and building understanding. This , join us in reaching out to someone dealing with the unseen challenges of chronic pain and show your support in the comments below. ⬇️

09/15/2025

In the (HS) community, you’re surrounded by people who get it. 💙​

HS can be painful, persistent, and often life-changing. But better science and stronger advocacy are helping change the story! We’re proud to stand with the HS community as we work to create solutions that lead to better days and less flare ups. To learn more about HS and how we’re working to be better advocates, visit https://bit.ly/45nmLVo

💚 Come together to learn more about thymidine kinase 2 deficiency (TK2d) and support the community.   is an ultra-rare g...
09/12/2025

💚 Come together to learn more about thymidine kinase 2 deficiency (TK2d) and support the community. is an ultra-rare genetic disease. ​

It affects each person differently, but everyone experiences muscle weakness. Other symptoms include fatigue, difficulty breathing, chewing and swallowing, and trouble speaking.​

Together, we can take on TK2d. Visit the link to find more information: https://bit.ly/3JUTQRq

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