Lilly-Humana data pact to focus on outcomes

Share this article:
William Fleming
William Fleming

Another drug maker is tapping Humana's claims database for therapeutic study. This time, it's Eli Lilly that wants to access de-identified medical, pharmacy and lab claims data from the payer to gauge the impact of interventions on outcomes and adherence programs, among other areas, according to a joint press release.

Under the terms of the multi-year agreement, the companies will conduct studies related to various disease states, starting with diabetes—a major source of revenue for the drug maker and of costs for the payer.

“Pairing Humana's clinical expertise and rich, de-identified patient data with Lilly's history and experience across many disease states allows us to maximize the potential benefits for patient care and savings,” said William Fleming, president of Humana Pharmacy Solutions.

Comprehensive Health Insights (CHI), a Humana subsidiary which specializes in crunching data assets for health economics and outcomes research (HEOR), will conduct the studies. Methodologies will also include disease management and pharmacoeconomics.

The Lilly deal follows Pfizer's 2011 pact with Humana, which involved real-world data and comparative-effectiveness research.

Initially, the retrospective analysis with Lilly will investigate patient characteristics associated with increased healthcare costs in people with type 2 diabetes.

“Working together, we hope to provide patients with insights and guidance that will help them tailor their care to best match their individual needs,” said Dara Schuster, MD, medical fellow, Lilly Diabetes.

Share this article:

Email Newsletters

More in Features

Leadership Exchange: How Do We Get Beyond the Pill?

Leadership Exchange: How Do We Get Beyond the ...

As its focus moves from manufacturing to service, pharma needs to partner with healthcare neophytes as well as established players. James Chase asks six experts to assess the risks and ...

FDA and off-label uses: a balancing act

FDA and off-label uses: a balancing act

FDA's current re-examination of its off-label promotion policies in light of the First Amendment is a delicate balancing act between its rock-solid traditional enforcement posture and a diverse new electronic ...

Read the complete August 2014 Digital Edition

Read the complete August 2014 Digital Edition

Click the above link to access the complete Digital Edition of the August 2014 issue of MM&M, with all text, charts and pictures.