H. Lundbeck A/S (Lundbeck) and Teva Pharmaceutical Industries Ltd. (NASDAQ: TEVA) have announced newly published long-term data on Azilect® (rasagiline tablets) from the TEMPO study and its open-label extension. The findings confirm the long-term efficacy, safety and tolerability of Azilect® in patients with Parkinson's disease (PD) and further demonstrate the benefits obtained with early treatment initiation. The data was published in the June 2010 issue of the International Journal of Neuroscience.

"The high proportion of patients (46%) remaining on Azilect® monotherapy after two years in the trial suggests that starting Azilect® earlier in the treatment paradigm offers us an effective and safe alternative to using dopamine agonists for an extended period of time," said Mark Lew, M.D., lead investigator and vice chair of the Department of Neurology and Director of the Division of Movement Disorders, Keck School of Medicine of the University of Southern California. "These results provide added support for a growing approach to treating patients with PD earlier in the course of their disease as was also shown in the ADAGIO study."

Two common PD assessment tools were used to analyze the TEMPO trial and its long-term extension - the Unified Parkinson's Disease Rating Scale (UPDRS), and the Hoehn & Yahr (H&Y) scale, both of which assess the severity of symptoms of PD and describe how they progress. Overall, the average annual increase in UPDRS score for all patients taking Azilect® (monotherapy or in combination with -additional dopaminergic therapies) was less than two UPDRS units a year (compared to an increase of 8-12 UPDRS scores per year, typically seen in untreated PD patients). At two years, 46% of patients remaining in trial were maintained on Azilect monotherapy. Additionally, only 25 percent of patients progressed to H&Y stage III by 5.4 years, thus demonstrating initial treatment with Azilect® is a viable and effective treatment option for early PD patients that is sustained in the long-term.

About the TEMPO trial and extension
The TEMPO [(TVP-1012) in Early Monotherapy for Parkinson's Disease Outpatients] trial and extension was a multicenter, double-blind, randomized, placebo-controlled, parallel group, delayed-start investigation of once-daily rasagiline in early Parkinson's disease. From the original cohort of 398 patients, 360 patients completed the double-blind phase of TEMPO, and 306 (85 percent) participated in the open-label extension. Patients were followed for up to 6.5 years with a mean of 3.5 ± 2.1 years. After 12 months, additional PD medications were added as required.

During the first 12 months of the study, participants received either rasagiline 1mg per day or rasagiline 2mg/day. During the extension phase, all subjects initially received rasagiline 2mg once daily. The dosing was changed to 1mg/day for all participants after six-month efficacy data showed no difference between the two doses.

Patients were examined approximately every three months during the extension phase. At each visit, the investigator recorded spontaneously reported adverse events (AEs) and assessed need for additional PD therapy. Azilect® was well-tolerated with 11.3 percent of patients (45/398) withdrawing because of an adverse event. The most common adverse events seen in this trial were infection, headache, nausea, dizziness, accidental injury and joint pain. Patients who withdrew because of an adverse event were as likely to be on Azilect® monotherapy (51 percent) as Azilect® combination therapy (49 percent).

About Azilect®
Azilect® tablets (rasagiline tablets) are indicated for the treatment of the signs and symptoms of Parkinson's disease both as initial monotherapy and as adjunct to levodopa later in the disease. Azilect® is currently available in 39 countries, including the US, Canada, Israel, Mexico, and all EU countries.

About Parkinson's disease
Parkinson's disease is an age-related degenerative disorder of the brain. Symptoms can include: tremor, stiffness, slowness of movement, and impaired balance. An estimated five million people worldwide suffer from the disease, with an average age of onset of about 60 years.

Lundbeck financial guidance
The content of this release will have no influence on the Lundbeck Group's financial guidance for 2010, which was provided on 4 March 2010 in connection with the release of the financial results for 2009.

About Teva
Teva Pharmaceutical Industries Ltd., (NASDAQ: TEVA) headquartered in Israel, is among the top 15 pharmaceutical companies in the world and is the leading generic pharmaceutical company. The company develops, manufactures and markets generic and innovative pharmaceuticals and active pharmaceutical ingredients. Over 80 percent of Teva's sales are in North America and Western Europe.

About Lundbeck
H. Lundbeck A/S (LUN.CO, LUN DC, HLUKY) is an international pharmaceutical company highly committed to improve the quality of life for people suffering from central nervous system (CNS) disorders. For this purpose Lundbeck is engaged in the research and development, production, marketing and sale of pharmaceuticals across the world, targeted at disorders like depression and anxiety, schizophrenia, insomnia, Huntington's, epilepsies, Alzheimer's and Parkinson's diseases.

Lundbeck was founded in 1915 by Hans Lundbeck in Copenhagen, Denmark, and employs today approximately 5,900 people worldwide. Lundbeck is one of the world's leading pharmaceutical companies working with CNS disorders. In 2009, the company's revenue was DKK 13.7 billion (approximately EUR 1.8 billion or USD 2.6 billion). For more information, please visit www.lundbeck.com.