Blog Coverage PTC Therapeutics Acquires Rights for Duchenne Muscular Dystrophy Drug from Marathon for $140 Million Upfront

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LONDON, UK / ACCESSWIRE / March 17, 2017 / Active Wall St. blog coverage looks at the headline from PTC Therapeutics, Inc. (NASDAQ: PTCT) as the Company announced on March 16, 2017, that it has entered into an asset purchase agreement with Marathon Pharmaceuticals, LLC to acquire all rights to Emflaza™ (deflazacort) for $140 million upfront. Emflaza is the first treatment approved in the United States for all Duchenne muscular dystrophy (DMD) patients five years and older, regardless of their genetic mutation. Register with us now for your free membership and blog access at:

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One of PTC Therapeutics' competitors within the Biotechnology space, NewLink Genetics Corp. (NASDAQ: NLNK), reported on February 28, 2017, its consolidated financial results for Q4 and year ended 2016. AWS will be initiating a research report on NewLink Genetics in the coming days.

Today, AWS is promoting its blog coverage on PTCT; touching on NLNK. Get all of our free blog coverage and more by clicking on the link below:

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"With our nearly 20-year commitment to the Duchenne community, it is deeply meaningful for us to bring this critical therapy to US patients," said Stuart W. Peltz, Ph.D., Chief Executive Officer of PTC Therapeutics, Inc., "We believe Emflaza is a disease-modifying therapy that has been shown to slow disease progression. In keeping with PTC's mission, we are excited to work with the community to raise the standard of care for DMD patients."

About Duchenne Muscular Dystrophy

Primarily affecting males, Duchenne muscular dystrophy (DMD) is a rare and fatal genetic disorder that results in progressive muscle weakness from early childhood and leads to premature death in the mid-twenties due to heart and respiratory failure. It is a progressive muscle disorder caused by the lack of functional dystrophin protein. Dystrophin is critical to the structural stability of skeletal, diaphragm, and heart muscles. Patients with DMD, the more severe form of the disorder, can lose the ability to walk as early as age ten, followed by loss of the use of their arms. DMD patients subsequently experience life-threatening lung complications, requiring the need for ventilation support, and heart complications in their late teens and twenties. DMD treatment guidelines recommend steroids as a foundational component of the standard of care. Emflaza reduces inflammation, which is critical to preserving muscle function and delaying disease progression. It received FDA approval on February 09, 2017 and has the potential to benefit many DMD patients in the US. However, the drug has been available outside the United States for decades.