Teva Announces AZILECT® (Rasagiline Tablets) Data To Be Presented At The 16th Annual International Congress Of Parkinson’s Disease And Movement Disorders
Teva Pharmaceutical Industries Ltd. (NYSE: TEVA) today announced that data from studies of AZILECT ® (rasagiline tablets) and Parkinson’s disease (PD) will be featured at the 16 th Annual International Congress of Parkinson’s Disease and Movement Disorders in Dublin, Ireland, 17-21 June 2012.
More than fifteen abstracts will highlight data from ongoing and completed studies of PD and AZILECT ®, a MAO-B inhibitor for the treatment of PD, in the areas of pre-clinical, clinical and health economics research.
“We are proud of the variety of topics and quality of research results that will be presented at MDS this year,” said Dr. Michael Hayden, President of Global R&D and Chief Scientific Officer, Teva Pharmaceutical Industries Ltd. “We are committed to ongoing collaboration with academia, medical institutions and patient advocacy groups to continue our understanding of the role AZILECT ® may play in the treatment landscape for the PD community – patients, their families and friends, and healthcare professionals.”
Presentations include:
Ongoing studies assessing effects of AZILECT ® treatment on motor and non-motor PD symptoms, both as monotherapy and when added to ongoing dopamine agonist therapy:- [345] Evaluating the Efficacy of Rasagiline on Depressive Symptoms and Cognition in Parkinson’s Disease Patients without Dementia: the ACCORDO Study (Session PD Clinical Trials: 18 June 2012 at 12:45 PM IST) Paolo Barone for the ACCORDO Study Investigators, Salerno, Italy
- [374] A Placebo-controlled, Randomized, Multicenter Study of Rasagiline as Add-on Therapy to Dopamine Agonists for Treatment of Early Parkinson’s Disease: the ANDANTE Study (Session PD Clinical Trials: 18 June 2012 at 12:45 PM IST) Robert Hauser, Tampa, FL,USA; Azhar Choudhry, Kansas City, MO, U.S.
- [450] A Comparative Study on Safety and Tolerability of Rasagiline Versus Pramipexole in Early Parkinson’s Disease: the ACTOR Study (Session PD Clinical Trials: 18 June 2012 at 12:45 PM IST) Francois Viallet, Provence, France, Severine Pitel, Marseille, France, Sylvie Lancrenon, Bourg la Reine, France, Oliver Blin, Marseille, France
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