If you're interested in answers to these and other questions about Sunovion, you're in the right place.
In October 2009, Sepracor Inc., a U.S. pharmaceutical company with a focus in CNS and Respiratory therapies, was acquired by Dainippon Sumitomo Pharma Co., Ltd. (DSP), a top ten, stock exchange-listed pharmaceutical company based in Osaka, Japan.
The move strengthened DSP's North American based drug development pipeline and commercial capabilities. And brought together extensive expertise in two main treatment categories—disorders of the central nervous system (CNS) and respiratory diseases.
In April 2010, DSP's original U.S. subsidiary, Dainippon Sumitomo Pharma America, Inc. (DSPA) was merged into Sepracor. Sunovion is the new company born of this union.
Sunovion isn't a household name. But we're confident that it will be. We believe our approach sets us apart. An approach characterized by two things.
First, we look beyond science for science's sake. We look at our patients' needs, and the needs of the healthcare professionals who care for them and find practical ways of developing better treatments.
Second, our focus on our patients' needs has led us to specialize in two distinct and broad-based areas of treatment. These days, more people in the United States from children to seniors are living with respiratory diseases. We are committed to improving their daily lives and helping to minimize the impact of their condition on their everyday activities.
We are equally committed to people suffering from disorders of the central nervous system. People with these conditions need new, advanced therapies to treat them effectively. And we're working to discover, develop and deliver the treatments they need. Sunovion's targeted discovery and development program has already resulted in several treatments such as LUNESTA® (eszopiclone), a medicine that helps people sleep better.
Other development programs under way at Sunovion are focused on treating CNS conditions like anxiety, depression, and epilepsy, and schizophrenia. Latuda® (lurasidone HCl) tablets was approved by the U.S. Food and Drug Administration (FDA) on October 28, 2010 for the treatment of patients with schizophrenia. LATUDA is available by prescription in pharmacies across the United States and Puerto Rico.