UCB on a Growth Path for a Decade+ Check out our Financial Performance Since 2015, UCB has embarked on a very important change journey: the Patient Value Strategy Our Strategic Growth Path Towards 2025 Disclaimer read more This website contains forward-looking statements, including, without limitation, statements containing the words “potential”, “believes”, “anticipates”, “expects”, “intends”, “plans”, “seeks”, “estimates”, “may”, “will”, “continue” and similar expressions. These forward-looking statements are based on current plans, estimates and beliefs of management. All statements, other than statements of historical facts, are statements that could be deemed forward-looking statements, including estimates of revenues, operating margins, capital expenditures, cash, other financial information, expected legal, arbitration, political, regulatory or clinical results or practices and other such estimates and results. 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Finally, a breakdown, cyberattack or information security breach could compromise the confidentiality, integrity and availability of UCB’s data and systems.Given these uncertainties, you are cautioned not to place any undue reliance on such forward-looking statements. These forward-looking statements are made only as of the date of this website, and do not reflect any potential impacts from the evolving conflicts, wars, pandemics, as well as any other adversity, unless indicated otherwise. The company continues to follow the development diligently to assess the financial significance of these events, as the case may be, to UCB.UCB expressly disclaims any obligation or duty to update any forward-looking statements in this website, either to confirm the actual results or to report or reflect any change in its forward-looking statements with regard thereto or any change in events, conditions or circumstances on which any such statement is based, unless such statement is required pursuant to applicable laws and regulations. close Our key medicines We bring solutions to people living with neurological or immunological diseases. Growth drivers BIMZELX® (bimekizumab) BIMZELX® (bimekizumab) Reaching more than 18 000 patients globally (Dec 2023)Indications: Psoriasis (PSO); Psoriatic Arthritis (PsA); Ankylosing spondylitis (AS); non-radiographic Axial Spondyloarthritis (nr-axSpA)Loss of Exclusivity (indicative): 2032 in U.S., without patent term extension; 2036 in Europe, 2037 in JapanSales: € 148 million in 2023Peak sales guidance: > € 4 billionBIMZELX® - prescribing information EVENITY® (romosozumab) EVENITY® (romosozumab) Reached more than 600 000 patients globally since launch (Dec 2023)Indication: OsteoporosisLoss of Exclusivity (indicative): 2031 in Europe and Japan, 2033 in U.S.Sales: € 60 million in 2023 in Europe. Net sales outside Europe reported by Amgen and AstellasEVENITY® - prescribing information FINTEPLA® (fenfluramine) FINTEPLA® (fenfluramine) Reaching more than 3 000 patients globally (Dec 2023)Indications: Dravet Syndrome, Lennox-Gastaut Syndrome. Loss of Exclusivity (indicative). 2032 in Europe and Japan, 2033 in U.S.Sales: € 226 million in 2023.Peak sales guidance: € 800 million by 2027.FINTEPLA® - prescribing information RYSTIGGO® (rozanolixizumab) RYSTIGGO® (rozanolixizumab) Launched in the U.S. in July 2023, approved in Europe and JapanIndication: generalized Myasthenia Gravis.Loss of Exclusivity (indicative): 2033 in Japan. 2034 in Europe and 2035 in U.S., all without patent term extension.Sales: € 19 million in 2023.RYSTIGGO® - prescribing information ZILBRYSQ® (zilucoplan) ZILBRYSQ® (zilucoplan) Global launches starting Q1/2024Indication: generalized Myasthenia Gravis.Loss of Exclusivity (indicative): 2035 in Europe, Japan & U.S. without patent term extension.ZILBRYSQ® - prescribing information Solid foundation BRIVIACT® (brivaracetam) BRIVIACT® (brivaracetam) Reaching more than 190 000 patients globally (MAT Q3/2023)Indication: Epilepsy partial-onset seizure, also known as focal seizureLoss of Exclusivity (indicative): 2026 in Europe & U.S.Sales: € 576 million in 2023Peak sales guidance: ≥ € 600 million by 2026BRIVIACT® - prescribing information CIMZIA® (certolizumab pegol) CIMZIA® (certolizumab pegol) Reaching more than 180 000 patients globally (MAT Q3/2023)Indications: Ankylosing spondylitis (AS); non-radiographic Axial Spondyloarthritis (nr-axSpA); Crohn's disease (CD); Psoriasis (PSO); Psoriatic arthritis (PsA); Rheumatoid arthritis (RA)Loss of Exclusivity (indicative): 2024 in Europe & U.S. 2026 in Japan.Sales: € 2 087 million in 2023Peak sales guidance: ≥ € 2 billion by 2024 achieved in 2022AS - prescribing informationnr-axSpA - prescribing informationCD - prescribing informationPSO - prescribing informationPsA - prescribing informationRA - prescribing information KEPPRA® (levetiracetam) KEPPRA® (levetiracetam) Reaching more than 1.7 million patients globally (MAT Q3/2023)Indications: Epilepsy partial-onset seizures, also known as focal seizures; Epilepsy primary generalized tonic-clonic seizures; Epilepsy myoclonic seizuresLoss of Exclusivity: U.S. - 2008, Europe - 2010, Japan - 2020.Sales: € 636 million in 2023Peak sales: € 1.2 billion (2008)KEPPRA® - prescribing information NAYZILAM® (midazolam nasal spray) NAYZILAM® (midazolam nasal spray) Reaching more than 70 000 patients in the U.S. (MAT Q3/2023)Indication: Epilepsy seizure clustersLoss of Exclusivity (indicative): 2028 in U.S.Sales: € 94 million in 2023NAYZILAM® - prescribing information VIMPAT® (lacosamide) VIMPAT® (lacosamide) Reaching more than 500 000 patients globally (MAT Q3/2023)Indications: Epilepsy partial-onset seizures, also known as focal seizures; Epilepsy primary generalized tonic-clonic seizuresLoss of Exclusivity: 2022 in Europe & U.S. 2024 in Japan (indicative)Sales: € 394 million in 2023Peak sales: € 1.5 billion (2021)VIMPAT® - prescribing information Our clinical development partnerships Press Release: Partnership with Amgen Press Release: Partnership with Biogen Press Release: Partnership with Novartis Press Release: Partnership with Cancer Research UK Our clinical development pipeline In a challenging environment, our pipeline builds the basis of UCB’s sustainable long-term growth. We continued to create value for patients, advancing our pipeline of potential solutions for severe diseases, expanding our capabilities by investing in state-of-the-art scientific platforms and medical advances, and further progress on our digital business transformation journey. General information All medicines must pass safety and efficacy tests if they are to be approved by regulators. This is done through a series of rigorous clinical studies, also referred to as clinical trials, research studies or medical research. Learn more Clinical studies index UCB is committed to sharing information on studies and making study results publicly accessible. You will find below links to the clinical studies (Phase 2-4) of our main R&D projects. Learn more Contact UCB IR Team investor-relations@ucb.com or a specific team member:Antje Witte, Head of Investor RelationsTel: +32 2 559 9414E-mail: Antje.Witte@ucb.com Sahar Yazdian, Investor Relations Lead Tel: +32 2 559 9137E-mail: Sahar.Yazdian@ucb.com Book a virtual meeting Send us feedback UCB IR App Choose a Country Global Site – English Australia – English België – Engels Belgique – Anglais Brasil – Português България – Български Canada – English Canada – Français 中国 – 中文 Česká Republika – Angličtina Danmark – Engelsk Deutschland – Deutsch France – Français España – Español Ελλάδα – Ελληνικά India – English Ireland – English Italia – Inglese 日本 – 日本語 한국 – 한국어 Luxembourg – Anglais Luxemburg – Engels Magyarország – Angol México & Latinoamérica – Español Nederland – Engels New Zealand – English Norge – Engelsk Österreich – Deutsch Polska – Polski Portugal – español y portugués România – Engleză Россия – Русский Slovensko – Anglický Suomi – Englanti Sverige – Engelska Schweiz – Deutsch Türkiye – Türkçe Україна – Англійська United Kingdom – English U.S.A. – English ×