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UCB SA NPV (UCBJF) Stock Price, News & Analysis

UCBJF OTC
Published by Stock Titan Data refreshed

Price Move History

Daily moves over 5%
42 230 sessions, November 4, 2025 to November 4, 2026
Largest daily move
+18.8% close of October 22, 2026
1-year change
+30.5% closing prices, November 4, 2025 to November 4, 2026
1-month change
+34.6% closing prices, October 2, 2026 to November 4, 2026

Company Description

UCB SA NPV (UCBJF) represents an interest in UCB, a global biopharmaceutical company based in Brussels, Belgium. According to company information, UCB focuses on the discovery and development of medicines and solutions for people living with severe diseases of the immune system or of the central nervous system. UCB is listed on Euronext Brussels under the symbol UCB.

Within the healthcare and biotechnology sector, UCB concentrates on serious, chronic conditions where there is a high unmet medical need. The company states that it aims to transform the lives of people affected by these diseases by advancing targeted therapies and scientific understanding of complex disorders. Its work spans research, clinical development and bringing approved medicines to patients in multiple countries.

Focus on Epilepsy and Severe Epileptic Conditions

Recent information highlights UCB’s extensive activity in epilepsy and developmental and epileptic encephalopathies (DEEs). The company reports presenting 26 scientific abstracts from its epilepsy portfolio at the International Epilepsy Congress, covering topics such as Dravet syndrome, Lennox-Gastaut syndrome, prolonged seizures, seizure emergencies and early pipeline research. This reflects a sustained focus on severe epileptic conditions that significantly affect quality of life for patients and caregivers.

UCB’s research includes long-term safety and global functioning data for FINTEPLA (fenfluramine) in children and adults with Dravet syndrome or Lennox-Gastaut syndrome, as well as studies on non-seizure impacts and caregiver experiences. The company also supports work on diagnostic challenges in DEEs, including qualitative studies of adult care settings and caregiver surveys on unpredictable seizures and disruptive behaviors. Additional analyses explore prolonged seizures, seizure duration cutoffs, seizure emergency pathways and the availability and reimbursement of acute seizure medications.

Central Nervous System and Immune System Diseases

Beyond epilepsy, UCB describes itself as focusing on severe diseases of the central nervous system and the immune system. This positioning indicates that its research and development efforts extend across multiple neurological and immunological conditions, although the detailed portfolio outside epilepsy is not elaborated in the provided information. The company emphasizes discovery and development activities intended to deliver medicines and related solutions for these patient populations.

Global Operations and Scale

UCB reports that it operates in approximately 40 countries and employs approximately 9,000 people worldwide. This geographic and organizational footprint supports its ability to conduct global clinical research, engage with healthcare professionals, and provide access to its medicines across different healthcare systems. The company also reports generating multi-billion-euro revenues, underlining its scale within the global biopharmaceutical industry.

Research, Clinical Evidence and Pipeline

The epilepsy-focused data presented by UCB spans clinical trials, open-label extension studies, retrospective claims analyses, caregiver surveys, qualitative research and early-stage laboratory work. For example, UCB highlights an open-label extension study of fenfluramine in Dravet syndrome and Lennox-Gastaut syndrome that reported no new or unexpected safety signals and long-term sustained benefit. Other work examines mortality in patients with these syndromes, family journeys, and tools to support diagnosis of Lennox-Gastaut syndrome.

UCB also reports early pipeline research in gene therapy and disease models related to STXBP1 haploinsufficiency, including AAV gene therapy in mouse models, in vitro rescue of neuronal activity using viral vectors, and electrophysiological studies of hippocampal network activity. Additional research addresses expression and quantification of STXBP1 splice variants in rodent and primate brain tissues. These efforts illustrate UCB’s interest in advancing mechanistic understanding and potential new therapeutic approaches for severe neurological disorders.

Medicines and Treatment Areas Highlighted

Within epilepsy, UCB’s materials reference FINTEPLA (fenfluramine) and brivaracetam. FINTEPLA is described in the EU as indicated for the treatment of seizures associated with Dravet syndrome and Lennox-Gastaut syndrome as an add-on therapy to other anti-epileptic medicines for patients 2 years of age and older, with initiation and supervision by physicians experienced in epilepsy treatment and prescribing under a controlled access programme. Brivaracetam is mentioned in relation to adjunctive therapy in pediatric and adult patients with focal-onset seizures in real-world settings.

These references underscore UCB’s engagement with both established therapies and ongoing evidence generation in real-world practice, as well as its interest in non-seizure outcomes, caregiver burden, and broader aspects of living with severe epileptic conditions.

Scientific and Medical Engagement

UCB’s presence at the International Epilepsy Congress includes oral presentations, poster abstracts and an industry-sponsored symposium titled "Time matters in developmental and epileptic encephalopathies." According to the company, this symposium aims to enhance knowledge and awareness of the broader impact of DEEs in adulthood, focusing on diagnosis, treatment journeys and barriers to care. This reflects UCB’s stated commitment to improving understanding of these complex conditions among clinicians and other stakeholders.

The company also collaborates with epilepsy experts from multiple countries to develop practical tools, such as a checklist to support diagnosis of Lennox-Gastaut syndrome for non-specialists, using established criteria as a framework. Such activities highlight UCB’s role in supporting clinical practice and contributing to consensus-building in challenging diagnostic areas.

Risk Factors and Forward-Looking Considerations

In its communications, UCB includes extensive cautionary language about forward-looking statements. The company notes that research and development outcomes, regulatory approvals, clinical trial timelines, safety findings, competitive dynamics, pricing and reimbursement policies, data security, and other factors can materially affect actual results compared to expectations. It emphasizes that movement from concept to commercial product is uncertain and that preclinical results do not guarantee safety and efficacy in humans.

This risk disclosure underscores the inherent uncertainty of biopharmaceutical research and the many external and internal factors that can influence product development, commercialization and financial performance.

Position Within the Healthcare and Biotechnology Sector

As a global biopharmaceutical company listed on a major European exchange and active in central nervous system and immune system diseases, UCB occupies a specialized position within the broader healthcare and biotechnology sector. Its emphasis on severe diseases, particularly in epilepsy and DEEs, aligns it with high-need therapeutic areas where clinical research is complex and long-term outcomes are crucial.

Investors and observers considering UCB SA NPV (UCBJF) can use this context to understand the company’s stated focus, therapeutic areas, and scientific activities, while recognizing the uncertainties and risks that UCB itself highlights in its public communications.

Stock Performance

$321.09
+1.96%
+6.17
Last updated: November 4, 2026 at 16:00
+30.5%
Performance 1 year
$61.2B

UCB SA NPV (UCBJF) closed at $321.09 on November 4, 2026. Over the past 12 months, the price has gained 30.5%.

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UCBJF Metrics & Rankings

Price returns through November 4, 2026. Month and year figures include the first trading day. Ranking links may use different dates.

Latest News

UCB SA NPV has 1 recent news article. Of the recent coverage, 0 articles coincided with positive price movement and 1 with negative movement. View all UCBJF news →

SEC Filings

No SEC filings available for UCBJF.

Short Interest History

Last 12 Months

Short interest in UCB SA NPV (UCBJF) currently stands at 1.0 million shares, down 14.9% from the previous reporting period, representing 0.8% of the float.

Days to Cover History

Last 12 Months

Days to cover for UCB SA NPV (UCBJF) currently stands at 1000.0 days. The ratio is the reported short interest divided by the average daily trading volume. Across the settlements charted above, it has ranged from 311.6 to 1000.0 days.

UCBJF Company Profile & Sector Positioning

UCB SA NPV (UCBJF) operates in the Biotechnology industry within the broader Healthcare sector and is listed on the OTC.

Investors comparing UCBJF often look at related companies in the same sector, including UCB SA (UCBJY), CSL Ltd (CSLLY), Genmab A/S DKK (GNMSF), WuXi Biologics (WXXWY), and Innovent Biolgcs (IVBIY). Comparing financial metrics, valuation ratios, and stock performance across these peers can help investors evaluate UCBJF's relative position within its industry.

Frequently Asked Questions

The current stock price of UCB SA NPV (UCBJF) is $321.09 as of November 4, 2026.

The market cap of UCB SA NPV (UCBJF) is approximately $61.2B. Learn more about what market capitalization means .

UCB SA NPV (UCBJF) represents an interest in UCB, a global biopharmaceutical company based in Brussels, Belgium. UCB focuses on discovering and developing medicines and solutions for severe diseases of the immune system and the central nervous system.

According to company information, UCB focuses on severe diseases of the immune system and of the central nervous system. Recent materials highlight extensive activity in epilepsy and developmental and epileptic encephalopathies, including Dravet syndrome and Lennox-Gastaut syndrome.

UCB is listed on Euronext Brussels under the symbol UCB. The UCB SA NPV (UCBJF) symbol reflects exposure to this underlying company.

UCB states that it has approximately 9,000 people in approximately 40 countries. This international footprint supports its research, clinical development and access to medicines across multiple regions.

UCB reports presenting 26 scientific abstracts from its epilepsy portfolio at the International Epilepsy Congress, covering Dravet syndrome, Lennox-Gastaut syndrome, prolonged seizures, seizure emergencies and early pipeline research. The company describes a commitment to improving care for people living with epilepsies and severe epileptic conditions.

FINTEPLA (fenfluramine) is referenced by UCB in relation to the treatment of seizures associated with Dravet syndrome and Lennox-Gastaut syndrome. In the EU, it is described as an add-on therapy to other anti-epileptic medicines for patients 2 years of age and older, initiated and supervised by physicians experienced in epilepsy treatment and prescribed under a controlled access programme.

UCB reports early pipeline research related to STXBP1 haploinsufficiency, including AAV gene therapy at neonatal age in mouse models, rescue of neuronal activity in iPSC-derived disease models using viral vectors, electrophysiological studies of hippocampal network activity, and analysis of STXBP1 splice variants in rodent and primate brain tissues.

UCB notes that forward-looking statements are based on current plans, estimates and beliefs, and that many known and unknown risks and uncertainties could cause actual results to differ materially. It cites factors such as regulatory approvals, research and development costs, clinical outcomes, competition, pricing and reimbursement policies, data security, and legal or political developments.

UCB states that it is committed to driving improvements in all aspects of care for people living with epilepsies and severe epileptic conditions. It aims to deepen insights into disease mechanisms, treatment outcomes and patient and caregiver experiences to help shape better futures for those affected.