SK life science launches new corporate presence, expanded commercial operations in the United States

December 1, 2017 | Friday | News

The company has launched a new corporate web site and plans to further unveil its new corporate brand and discuss its pipeline and commercialization strategy at the American Epilepsy Society's annual meeting in Washington, D.C.

Source: Flickr

Source: Flickr

SK Life Science, Inc., a subsidiary of SK Biopharmaceuticals Co., Ltd., an innovative biopharmaceutical company focused on developing and bringing to market treatments for disorders of the central nervous system (CNS), today announced the launch of its commercial corporate presence and infrastructure in the United States.

With a strong pipeline of products focused on potential treatments for disorders such as epilepsy, sleep disorder and attention deficit hyperactivity disorder, SK life science is working to redefine the future of CNS therapies with products that may make a difference in the lives of patients.

The company has launched a new corporate web site and plans to further unveil its new corporate brand and discuss its pipeline and commercialization strategy at the American Epilepsy Society's annual meeting in Washington, D.C., from Dec. 1 – 5, 2017.

SK life science and its parent company SK biopharmaceuticals, were founded in 1993 with a focus on research and development and building strategic partnerships driven by the needs of patients, healthcare professionals, caregivers and the CNS community. The company has initiated 16 Investigational New Drug (IND) applications with the U.S. Food and Drug Administration (FDA) and has entered into licensing and development agreements with multiple global pharmaceutical companies.

Today, SK life science has a pipeline of six projects in development, with its lead compound, cenobamate, an investigational product, currently in Phase III development for the potential treatment of patients with epilepsy. In 2015, SK life science reached an agreement with the FDA that their two adequate and well-controlled Phase II studies would appear sufficient to support the filing of a New Drug Application.

 

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