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Sandoz Sues Amgen Over Chemo Syringe Marketing

Sandoz Inc. filed a complaint against Amgen Inc. and Amgen Manufacturing Limited, alleging the defendants engaged in false advertising and unfair

Real-time TA curve in column chromatography with SIMCA®

Real-time TA curve in column chromatography with SIMCA®
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Functional Antibody Claims: Setting the Bar for Enablement | Locke Lord LLP

To embed, copy and paste the code into your website or blog: On February 11, 2021, in a unanimous decision, the Federal Circuit affirmed the district court’s holding that Amgen Inc., Amgen Manufacturing, Ltd., and Amgen USA, Inc.’s (collectively, “Amgen’s”) antibody composition claims are invalid for lack of enablement.  Amgen Inc. v. Sanofi, Aventisub LLC, No. 20-1074 (Fed. Cir. 2021).  The patented technology relates to an antibody composition for treating high levels of cholesterol in the blood or hypercholesterolemia.  See id. at 3.  A high level of low-density lipoprotein (“LDL”) cholesterol, often called “bad” cholesterol, is associated with heart disease.  Id.  LDL receptors (“LDLRs”), present on the surface of cells, bind to LDL cholesterol in the blood and regulate the amount of circulating LDL cholesterol.  

Federal Circuit Resolves Pharma Companies Patent Battle in Favor of Sanofi

Health your username February 12, 2021 In a suit brought by Amgen Inc., Amgen Manufacturing, Ltd., and Amgen USA, Inc. (collectively, Amgen) against Sanofi, Aventisub LLC, Regeneron Pharmaceuticals Inc., Sanofi-Aventis U.S. LLC (collectively, Sanofi) more than six years ago, the Federal Circuit has affirmed the district court’s determination that certain Amgen patent claims were invalid for lack of enablement. The asserted claims of Amgen’s two patents describe antibodies that help the body regulate low-density lipoprotein cholesterol (LDL). According to Thursday’s opinion, this was the second time the patents have been before the Federal Circuit. The present dispute concerned whether Amgen’s asserted claims were invalid for lack of enablement. In order to pass the federal enablement requirement, the court explained, the question is whether one reasonably skilled in the art could make or use the invention from the disclosures in the patent coupled with informa

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