Ambry Genetics
1 Enterprise
Aliso Viejo, CA 92656
ALISO VIEJO, Calif.--(BUSINESS WIRE)--Ambry Genetics, the worldwide leader in hereditary cancer testing, announced today that it has filed an antitrust counterclaim against Myriad Genetics in response to the patent infringement lawsuit Myriad and other plaintiffs filed against Ambry on July 9, 2013, University of Utah Research Foundation, et al, v. Ambry Genetics Corporation, United States District for the District of Utah, Case No. 2:13-cv-00640-RJS.
Ambry's antitrust counterclaim alleges that:
Ambry Genetics was the first commercial laboratory to launch hereditary cancer panels using next generation sequencing in 2012 with their comprehensive BreastNext, OvaNext, ColoNext and CancerNext products. With hundreds of clinics and institutions utilizing these panels, Ambry has established itself as the scientific leaders in inherited cancer panel testing. Following the Supreme Court’s landmark June 13, 2013 decision in AMP et al v. Myriad Genetics, et al., Ambry included BRCA1 and BRCA2 diagnostic testing to its suite of panels.
“Being sued for patent infringement a month after the Supreme Court ruled 9-0 unanimously against Myriad is just wrong,” said Chief Executive Officer, Charles Dunlop. “As alleged in our counterclaim, Myriad Genetics is also wrongfully depicting Ambry’s variants of unknown significance (VUS) statistic to be as high as 30% when it actually is approximately 5% for BRCA1/2 diagnostic testing. Tactics like this have no place in the medical field, especially cancer, as it will take a collaborative, industry wide effort to further understand the disease and find cures.”
About Ambry Genetics®
Ambry's antitrust counterclaim alleges that:
Ambry Genetics was the first commercial laboratory to launch hereditary cancer panels using next generation sequencing in 2012 with their comprehensive BreastNext, OvaNext, ColoNext and CancerNext products. With hundreds of clinics and institutions utilizing these panels, Ambry has established itself as the scientific leaders in inherited cancer panel testing. Following the Supreme Court’s landmark June 13, 2013 decision in AMP et al v. Myriad Genetics, et al., Ambry included BRCA1 and BRCA2 diagnostic testing to its suite of panels.
“Being sued for patent infringement a month after the Supreme Court ruled 9-0 unanimously against Myriad is just wrong,” said Chief Executive Officer, Charles Dunlop. “As alleged in our counterclaim, Myriad Genetics is also wrongfully depicting Ambry’s variants of unknown significance (VUS) statistic to be as high as 30% when it actually is approximately 5% for BRCA1/2 diagnostic testing. Tactics like this have no place in the medical field, especially cancer, as it will take a collaborative, industry wide effort to further understand the disease and find cures.”
About Ambry Genetics®
Ambry Genetics translates scientific research into clinically actionable test results based upon a deep understanding of the human genome and the biology behind genetic disease. It is a leader in genetic testing that aims to improve health by understanding the relationship between genetics and disease. Its unparalleled track record of discoveries over 20 years, and growing database that continues to expand in collaboration with academic, corporate, and pharmaceutical partners, means Ambry Genetics is first to market with innovative products and comprehensive analysis that enable clinicians to confidently inform patient health decisions.
Contacts
For Ambry Genetics
gwen@gwengordonpr.com