UCB on a Growth Path for a Decade+ Check out our Financial Performance UCB’s Decade+ of Growth: Elevating lives of people through our medicines 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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There is no guarantee that new product candidates will be discovered or identified in the pipeline, or that new indications for existing products will be developed and approved. Movement from concept to commercial product is uncertain; preclinical results do not guarantee safety and efficacy of product candidates in humans. So far, the complexity of the human body cannot be reproduced in computer models, cell culture systems or animal models. The length of the timing to complete clinical trials and to get regulatory approval for product marketing has varied in the past and UCB expects similar unpredictability going forward. Products or potential products which are the subject of partnerships, joint ventures or licensing collaborations may be subject to disputes between the partners or may prove to be not as safe, effective or commercially successful as UCB may have believed at the start of such partnership. UCB’s efforts to acquire other products or companies and to integrate the operations of such acquired companies may not be as successful as UCB may have believed at the moment of acquisition. Also, UCB or others could discover safety, side effects or manufacturing problems with its products and/or devices after they are marketed. The discovery of significant problems with a product similar to one of UCB’s products that implicate an entire class of products may have a material adverse effect on sales of the entire class of affected products. Moreover, sales may be impacted by international and domestic trends toward managed care and health care cost containment, including pricing pressure, political and public scrutiny, customer and prescriber patterns or practices, and the reimbursement policies imposed by third-party payers as well as legislation affecting biopharmaceutical pricing and reimbursement activities and outcomes. Finally, a breakdown, cyberattack or information security breach could compromise the confidentiality, integrity and availability of UCB’s data and systems.Given these uncertainties, the public is 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 document, and do not reflect any potential impacts from the evolving event or risk as mentioned above 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 to update any forward-looking statements in this document, 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) Reaching more than >116 000 patients globally in 2025Indications: Psoriasis (PSO); Psoriatic Arthritis (PsA); Ankylosing spondylitis (AS); non-radiographic Axial Spondyloarthritis (nr-axSpA), hidradenitis suppurativa (HS)Loss of Exclusivity (indicative): 2035 in U.S., without patent term extension; 2036 in Europe, 2037 in JapanSales: € 2.2bn million in FY 2025Peak sales guidance: > € 4 billionBIMZELX® - prescribing information EVENITY® (romosozumab) Reached more than 1 300 000 patients globally since launch Indication: OsteoporosisLoss of Exclusivity (indicative): 2031 in Europe and Japan, 2033 in U.S.Sales: € 137 million in FY 2025 in Europe. Net sales outside Europe reported by Amgen and AstellasEVENITY® - prescribing information FINTEPLA® (fenfluramine) Reaching more than 14 000 patients globally Indications: Dravet Syndrome, Lennox-Gastaut Syndrome. Loss of Exclusivity (indicative). 2032 in Europe and Japan, 2033 in U.S.Sales: € 427 million in FY 2025.Peak sales guidance: € 800 million by 2027.FINTEPLA® - prescribing information RYSTIGGO® (rozanolixizumab) Launched in the U.S. in July 2023, approved and launched in Europe and JapanIndication: generalized Myasthenia Gravis.Loss of Exclusivity (indicative): 2037 in Japan. 2034 in Europe and 2035 in U.S., all without patent term extension.Sales: € 332 million in FY 2025.RYSTIGGO® - prescribing information ZILBRYSQ® (zilucoplan) Global launches started April 2024Indication: generalized Myasthenia Gravis.Loss of Exclusivity (indicative): 2035 in Europe, U.S. without patent term extension. Japan 2040.Sales: € 217 million in FY 2025ZILBRYSQ® - prescribing information Solid foundation BRIVIACT® (brivaracetam) Indication: Epilepsy partial-onset seizure, also known as focal seizureLoss of Exclusivity (indicative): 2026 in Europe & U.S. and 2034 in JapanSales: €758 million in FY 2025Peak sales guidance: ≥ € 600 million by 2026, reached 2 years ahead of timeBRIVIACT® - prescribing information CIMZIA® (certolizumab pegol) 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): 2026 in Japan.Sales: € 1 954 million in FY 2025 KEPPRA® (levetiracetam) Indications: Epilepsy partial-onset seizures, also known as focal seizures; Epilepsy primary generalized tonic-clonic seizures; Epilepsy myoclonic seizuresSales: € 439 million in FY 2025KEPPRA® - prescribing information NAYZILAM® (midazolam nasal spray) Indication: Epilepsy seizure clustersLoss of Exclusivity (indicative): 2028 in U.S.Sales: € 128 million in FY 2025NAYZILAM® - prescribing information VIMPAT® (lacosamide) 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 Sales: € 303 million in FY 2025VIMPAT® - prescribing information Our clinical development partnerships Press Release: Partnership with Amgen Press Release: Partnership with Biogen Press Release: Partnership with Cancer Research UK Our clinical development pipeline UCB remains committed to innovation, continuously seeking new ways to deliver meaningful solutions for people living with severe immunological and neurological conditions. This commitment is reflected in its robust clinical development pipeline, which currently includes one post-approval (Phase 4) asset, one asset in submission, and a diversified portfolio of four Phase 3 and three Phase 2 programs targeting distinct patient populations. Also in 2025, UCB has initiated three global Phase 3 studies for bimekizumab in pediatric indications: psoriasis, hidradenitis suppurativa, and juvenile idiopathic arthritis. In addition, the company plans to launch in 2026 a phase 3 program with fenfluramine for patients with Rett-syndrome and a phase 3 program with rosanolixizumab in ocular myasthenia gravis (oMG). UCB will explore the potential of galvokimig in respiratory diseases: two respiratory indications, Chronic Obstructive Pulmonary Disease (COPD) and non-cystic fibrosis bronchiectasis (NCFB), with respective proof of concept studies (phase 2a) are starting later in 2026. 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 Yvonne Naughton, Head of Investor RelationsTel: +44-175-344 7521E-mail: Yvonne.Naughton@ucb.comSahar Yazdian, Investor Relations Lead Tel: +32 2 559 9137E-mail: Sahar.Yazdian@ucb.com Diyana Mishu, Investor Relations ManagerTel: +32 2 599 7446E-mail: Diyana.Mishu@ucb.com Book a virtual meeting Send us feedback UCB IR App