Migraine class value-based contracts drive quality and value to payers and patients for Emgality® and REYVOW®
Contracts measure member outcomes and costs
December 4, 2020
Two migraine medications by Lilly, Emgality® and REYVOW®, have been Food and Drug Administration (FDA) approved in the past two years. In the highly competitive migraine drug class, Prime and Lilly found a new opportunity with these recently approved medicines to gather data from Prime’s real-world population around cost and patient outcomes through value-based contracting.
Separate value-based contracts were developed for Emgality and REYVOW. Both contracts measure members’ costs while the Emgality value-based contract also measures member outcomes.
Migraine is the third most prevalent disease in the world, with 12% of the population suffering from it. According to the Medical Expenditures Panel Survey, the total unadjusted cost among patients with migraine in the U.S. is estimated to be as high as $56 billion annually.²
“Driving to high value and affordable cost of medicines is top priority for our health plan clients and members,” said Kelly McGrail-Pokuta, vice president, pharmaceutical trade relations at Prime. “These value-based contracts create a measurable agreement with Lilly that we will see positive results from their medications.”
Libby Driscoll, vice president of Lilly Neurosciences, shared, “We are committed to providing novel treatments for people battling migraine, a prevalent yet under-recognized, debilitating disease. We’re pleased to partner with Prime to ensure access to our innovative and effective medicines including Emgality and REYVOW. By partnering with Prime on these agreements, we confidently stand behind the value our migraine medicines offer patients in a real-world setting and the value they deliver for the health system.”
See this whitepaper from July 2020 to learn more about how Prime and Lilly work together to support patient-centered value-based arrangements for prescription drugs.
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