Merck acknowledges the U.S. Department of Veterans Affairs for adopting biosimilar medicines to increase treatment options for veterans

Merck/MSD

4 October 2018 - Merck acknowledged the U.S. Department of Veterans Affairs for adopting biosimilar medicines as a means of increasing biologic medicine options for Veterans. 

Merck’s biosimilar Renflexis (infliximab-abda) was determined to be the lowest priced offer and was awarded a national contract, therefore it is the infliximab product available on the Veterans Affairs National Formulary.

“We are pleased that VA has chosen to expand access to an important treatment option such as RENFLEXIS for our Veterans who have nobly served this country,” said Patrick Magri, senior vice president, U.S. Hospital & Specialty Business Unit, Merck.

Renflexis was approved by the U.S. FDA in April 2017 as a biosimilar to Remicade (infliximab).

Read Merck press release

Michael Wonder

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Michael Wonder