Vizient Commends the FDA on Its Recent Approval of the First Neulasta Biosimilar
IRVING, Texas--(BUSINESS WIRE)--Jun 5, 2018--Vizient today applauds the U.S. Food and Drug Administration (FDA) on its announcement yesterday that it approved the first biosimilar to Neulasta (pegfilgrastim) and the overall progress in authorizing more competing versions of commonly used, high cost biologics.
Vizient has long been a vocal proponent of biosimilar approval, adoption and use and has continued to provide education to encourage understanding of this developing market. Vizient recently published a blog on the subject, as well as a letter in the Journal of Clinical Oncology titled “Clarifying Our Understanding of Biosimilars in Oncology: Response to ASCO Statement.” Biosimilar competition strengthens the healthcare market via increasing access to biologic therapy through lowering costs for patients and providers.
The FDA defines a biosimilar as, “a biological product that is highly similar to and has no clinically meaningful differences from an existing FDA-approved reference product.” While more streamlined than the approval pathway for originators, a biosimilar evaluation is both thorough and rigorous and maximizes the capabilities of analytical characterization to yield a product that is highly similar to the reference biologic in terms of safety, purity and potency.
Additionally, biosimilars approved in highly regulated markets like the U.S. and in Europe, have yielded the same clinical performance as their branded, originator counterparts. Therefore, we believe biosimilars have the potential to significantly lower the expense for biologic drugs that are currently cost prohibitive for many, while simultaneously maintaining a high level of quality and improved clinical outcomes.
Vizient is the nation’s largest health care performance improvement company serving a diverse membership that includes academic medical centers, pediatric facilities, community hospitals, integrated health care delivery networks and non-acute health care providers.
About Vizient, Inc.
Vizient, Inc., the largest member-driven health care performance improvement company in the country, provides innovative data-driven solutions, expertise and collaborative opportunities that lead to improved patient outcomes and lower costs. Vizient’s diverse membership base includes academic medical centers, pediatric facilities, community hospitals, integrated health delivery networks and non-acute health care providers and represents approximately $100 billion in annual purchasing volume. The Vizient brand identity represents the integration of VHA Inc., University HealthSystem Consortium and Novation, which combined in 2015, as well as MedAssets’ Spend and Clinical Resource Management (SCM) segment, including Sg2, which was acquired in 2016. In 2018, Vizient again received a World’s Most Ethical Company designation from the Ethisphere Institute. Vizient’s headquarters are in Irving, Texas, with locations in Chicago and other cities across the United States. Please visit www.vizientinc.com as well as our newsroom, blog, Twitter, LinkedIn and YouTube pages for more information about the company.
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CONTACT: Vizient, Inc.
Angie Boliver, 972-830-7961
KEYWORD: UNITED STATES NORTH AMERICA TEXAS
INDUSTRY KEYWORD: PRACTICE MANAGEMENT HEALTH BIOTECHNOLOGY HOSPITALS PUBLIC POLICY/GOVERNMENT HEALTHCARE REFORM ONCOLOGY OTHER POLICY ISSUES FDA MEDICAL SUPPLIES
SOURCE: Vizient, Inc.
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PUB: 06/05/2018 03:11 PM/DISC: 06/05/2018 03:11 PM