UCB USA

08/22/2025

This week’s Raleigh Town Hall at Research Triangle Park was a blast!💙
We brought together leaders and colleagues from across the U.S. — as well as local government partners from Governor Josh Stein's team — to bridge the gap between research and real-world patient impact. From behind-the-scenes science to meaningful discussions about how we elevate lives, the energy was uplifting and rooted in one shared mission: putting patients at the center of everything we do.

We left inspired and ready to keep pushing the boundaries of patient-centric innovation.

08/18/2025

Planning for the future can be one of the most challenging parts of caregiving. We're proud to partner with LGS Foundation to provide the C.A.R.E. Binder to help families like the Groff's navigate their journey. Read their story via USA TODAY: https://bit.ly/4mPaVdQ

These parents have two worst nightmares: They outlive their son, or their son outlives them. This is the reality for the Groff family.

Their 39-year-old son Danny has a rare and severe type of epilepsy and needs 24/7 care. The two 66-year-old retired educators are terrified at the possibility that he outlives them.

08/16/2025

🧬 4 Ways UCB Is Reimagining Care for Severe & Rare Diseases 💡​

1. Transformative Soultions Across 4 Focus Areas​
💙 Epilepsy & Rare Syndromes: Including Lennox-Gastaut syndrome (LGS), Dravet syndrome
💙 Dermatology: Treating plaque psoriasis (PSO), psoriatic arthritis (PsA) and hidradenitis suppurativa (HS).​
💙 Rheumatology: Focused on PsA, axial spondyloarthritis (axSpA), non-radiographic axial spondyloarthritis (nr-axSpA) and rheumatoid arthritis (RA).​
💙 Rare Diseases: Advancing treatment for generalized myasthenia gravis (gMG)

2. Patient-Driven Innovation: We invest in science, targeting root causes to deliver more personalized care and meet unmet needs.​

3. Advocacy in Action: Partnering with communities to amplify patient stories, fight stigma & expand access to care.​

4. Equity in Access: Through affordability, education & support services, we help ensure every patient can access treatment.​

➡️ Learn how we’re driving impact in neurology, immunology & rare diseases at https://bit.ly/4mfuJa9

08/15/2025

We’re UCB, of course we’re here for the HS community! 💙

08/14/2025

To us, wellness isn’t just a perk, it’s part of how we lead. Feeling balanced is the key foundation for doing our best work for the communities we serve. 💙​

This National Wellness Month, we’re celebrating the ways we foster a wellness culture that supports our employees, at work and beyond:​

💻 Flexible hybrid work​
🏋️ In-house gym​
💺 Office massage chairs​
🧘‍♀️ Employee access to wellness apps and features

08/12/2025

We don’t just meet expectations. We exceed them, holding ourselves to higher standards to deliver better outcomes for people living with severe diseases. Read more about our commitment to accessible treatments and how UCB’s growth is making a positive impact. https://bit.ly/4167Eyd

08/11/2025

Psoriasis is more than skin deep, and for Richard Van, it has shaped everything from his early healthcare experiences to his career today.

Richard knowns firsthand what it’s like to have both Psoriasis and Psoriatic Arthritis, and now, he uses these insights to drive change. Here at UCB, he leads global data initiatives to help improve the lives of patients like him – because often, those living with rare and severe disease are the best advocates. 💙

This , we’re proud to support the National Psoriasis Foundation in raising awareness for the 8M+ people in the U.S. living with psoriatic disease.

http://bit.ly/45MtV6U

08/06/2025

🌟 It’s one thing to talk about supporting families — it’s another to see it in action.​

Camp Small Steps brings that purpose to life by creating space for connection, joy, and community for families navigating life with Dravet syndrome.​

In this video, hear directly from UCB employees about why moments like these matter and why they’re proud to be part of the journey.​

Watch now and learn more at ShineForwardWithDravet.com. 💜🏕️​

08/05/2025

Powerful conversations. Inspiring workshops. Bringing the Hidradenitis Suppurativa (HS) community together. Driving real change.​

The HS Summit showcased how we’re working hand-in-hand with the HS community by listening, learning, and leading to create better solutions for those living with this chronic condition. 💙​

Our mission is simple: to bring hope, connection, and real progress for people living with HS. Learn more about our HS Summit: https://bit.ly/45nmLVo

07/30/2025

Our interns bring fresh ideas, energy, and real impact to the work we do, helping us build a brighter future for people living with rare and severe diseases.

Want to make a difference with us? Learn more about our internship opportunities: https://bit.ly/4lWUmN1

07/22/2025

Serving our communities is at the heart of who we are. 💙​
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This week, we partnered with Hands On Atlanta to pack STEAM kits for students with limited resources. As we work to create opportunities and elevate lives, empowering the next generation of thinkers, problem-solvers, and innovators right here in Atlanta is one of the ways we bring this commitment to action.​ Learn more about our work with Hands On Atlanta at https://bit.ly/4kV2T1D

07/21/2025

When her granddaughter Rosie was diagnosed with Dravet syndrome, Melanie became a caregiver, advocate, and voice for the rare disease community.

We’re proud to partner with the Dravet Syndrome Foundation and work alongside families like Melanie’s through our Shine Forward With Dravet program and community events like Camp Small Steps, part of our ongoing commitment to raising awareness and strengthening support for those living with Dravet syndrome and their loved ones.

Hear Melanie’s story on RARECast via Global Genes: https://bit.ly/46kSVmD