Last €68.39 EUR
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08/29/14 - €75.40
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ucb sa (UNC) Details

UCB S.A., a biopharmaceutical company, focuses on various diseases in therapeutic areas of neurology and immunology in Belgium and internationally. The company’s products include Cimzia for Crohn’s disease, rheumatoid arthritis, psoriatic arthritis, and axial spondyloarthritis/ankylosing spondylitis; Vimpat for the treatment of partial-onset seizures; and Neupro for Parkinson’s disease and restless legs syndrome. It also offers Keppra for epilepsy; Zyrtec and Xyzal for allergy; Metadate for attention deficit and hyperactivity disorders; Nootropil for the treatment of vertigo and events associated with ageing; and Xyrem for narcolepsy. In addition, the company provides Tussionex for relief of cough and upper respiratory symptoms associated with allergy or a cold; and Lortab for the relief from pain. The company’s development stage products include brivaracetam as adjunctive therapy for epilepsy; tozadenant for Parkinson’s disease; epratuzumab for systemic lupus erythematosus; romosozumab for osteoporosis; UCB4940 for psoriatic arthritis; UCB5857 and UCB7665 for immunological diseases; UCB4942 for drug resistant epilepsy; and dapirolizumab pegol for systemic lupus erythematosus. It has strategic alliances with the Weill Cornell Medical College (U.S.), Sanofi, and Dermira Inc., as well as collaboration and agreement with Neuropore Therapies Inc. UCB S.A. was founded in 1928 and is headquartered in Brussels, Belgium.

8,535 Employees
Last Reported Date: 02/28/15
Founded in 1928

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ucb sa (UNC) Key Developments

UCB Announces Earnings Results for the Financial Year 2014; Provides Earnings Guidance for the Year 2015

UCB announced earnings results for the financial year 2014. For the year, the company reported that revenues increased by 7% year on year (y/y) on a reported basis to EUR 3.3 billion. Net sales were up 5% y/y to EUR 2.9 billion. In particular, the company's core product portfolio - Cimzia (certolizumab), Vimpat (lacosamide), and Neupro (rotigotine) accounted for 50% of overall company sales and boosted company performance by bringing combined sales growth of 24% y/y, edging up to EUR 1.5 billion. The company provided earnings guidance for the year 2015. Looking at the financial outlook published by the company, the firm is confident that the core portfolio of products will continue to deliver sustained growth in 2015. In particular, the company forecasted achieving revenues of approximately EUR 3.55 billion to EUR 3.65 billion. Furthermore, recurring EBITDA is expected to attain EUR 710 million to -740 million.

UCB S.A., 2014 Earnings Call, Feb 27, 2015

UCB S.A., 2014 Earnings Call, Feb 27, 2015

UCB S.A. Announces Positive Results from Two Phase III Parkinson's Disease Studies

UCB S.A. has announced positive results from two Phase III studies evaluating Neupro, or rotigotine transdermal patch, in the treatment of patients in China with early- and advanced-stage idiopathic Parkinson's disease. Results from the Phase III study in patients with early-stage Parkinson's disease demonstrated that rotigotine transdermal patch significantly improved symptoms when compared to placebo. In addition, data from the Phase III study in advanced Parkinson's disease showed that patients treated with rotigotine had a significantly greater decrease in their 'off' time, or periods of poor mobility, slowness and stiffness, compared to those patients taking placebo. The adverse event profile observed in these studies and in this Chinese population were consistent with that known for rotigotine. One of the two Phase III studies was a multicenter, randomized, double-blind, parallel-group, placebo-controlled, 24-week study that evaluated the efficacy and safety of rotigotine (escalating weekly dose starting with daily doses of 2 mg/24 hours to 8 mg/24 hours) in 247 adult patients (30 years and older) with early-stage idiopathic Parkinson's disease. The primary efficacy variable was the change in the sum of the score from the Activities of Daily Living scale and motor examination in the Unified Parkinson's Disease Rating Scale (UPDRS) from baseline to the end of the maintenance period. The second Phase III study was a multicenter, randomized, double-blind, parallel-group, placebo-controlled, 12-week study that evaluated the efficacy and safety of rotigotine (escalating weekly dose starting with daily doses of 4 mg/24 hours to 16 mg/24 hours) in 346 adult patients (30 years and older) with advanced-stage idiopathic Parkinson's disease who were not well-controlled on levodopa.


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Price/Sales 3.6x
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