UCB SA (ETR:UNC)

Germany flag Germany · Delayed Price · Currency is EUR
237.50
+1.80 (0.76%)
At close: May 12, 2026
Market Cap45.93B +42.4%
Revenue (ttm)7.74B +25.8%
Net Income1.56B +46.3%
EPS8.03 +46.5%
Shares Outn/a
PE Ratio29.48
Forward PE22.44
Dividend1.02 (0.44%)
Ex-Dividend DateMay 4, 2026
Volume55
Average Volume76
Open237.50
Previous Close235.70
Day's Range237.50 - 237.50
52-Week Range203.00 - 287.20
Betan/a
RSI44.45
Earnings DateJul 30, 2026

About UCB SA

UCB SA, a biopharmaceutical company, develops products and solutions for people with neurology and immunology diseases worldwide. The company offers Cimzia for ankylosing spondylitis (AS), axial spondyloarthritis, Crohn's disease, non-radiographic axial spondyloarthritis, plaque psoriasis, psoriatic arthritis, polyarticular juvenile idiopathic arthritis, and rheumatoid arthritis; Vimpat, Keppra, and Briviact for epilepsy; and Neupro for Parkinson’s disease and restless legs syndrome. It also provides Nayzilam, a nasal spray rescue treatment for... [Read more]

Industry Biological Products, Except Diagnostic Substances
Founded 1925
Employees 9,765
Stock Exchange Deutsche Börse Xetra
Ticker Symbol UNC

Financial Performance

In 2025, UCB SA's revenue was 7.74 billion, an increase of 25.83% compared to the previous year's 6.15 billion. Earnings were 1.56 billion, an increase of 46.29%.

Financial Statements

News

UCB to Buy Candid Therapeutics for Up to $2.2 Billion

The deal seeks to bolster the company's pipeline of experimental treatments for autoimmune and inflammatory diseases.

9 days ago - WSJ

Belgian pharma group UCB to buy Candid Therapeutics for up to $2.2 billion

Belgian biopharmaceuticals company ​UCB has ‌agreed to buy privately-held Candid ​Therapeutics in ​a deal worth ⁠up to $2.2 ​billion, the companies ​said on Sunday.

10 days ago - Reuters

Belgium's UCB in autoimmune drug deal with Antengene

Belgian drugmaker UCB has entered into an agreement to licence Antengene's experimental autoimmune ​disease therapy ATG-201 and associated ‌technology, paying $60 million up front and over $1.1 billio...

2 months ago - Reuters

U.S. FDA approves KYGEVVI® (doxecitine and doxribtimine), the first and only treatment for adults and children living with thymidine kinase 2 deficiency (TK2d)

Approved indication: KYGEVVI® (doxecitine and doxribtimine) powder for oral solution (2g/2g) is approved for the treatment of thymidine kinase 2 deficiency (TK2d) in adults and pediatric patients with...

6 months ago - PRNewsWire