Merck has reported data from an observational study that assessed the differences in initiated insulin therapy in patients with type 2 diabetes taking a combination of Januvia (sitagliptin) and metformin, as well as sulphonylurea and metformin.

The study found that patients administered with a combination of sitagliptin and metformin initiated insulin therapy at a slower rate than patients treated with sulphonylurea and metformin.

The study used a propensity score matched sample from the GE Centricity Electronic Medical Record database.

"Due to the methods employed in this analysis, the time period in which an outcome can be observed must be prespecified and patients without complete data needed to be excluded."

Under the study, initially 7,728 patients with type 2 diabetes were administered with sitagliptin or sulphonylurea as dual therapy with metformin for at least 90 days after starting sitagliptin or sulphonylurea in 2006 to 2013.

The company used the Kaplan-Meier estimator to find out the progression to insulin use between the groups using sitagliptin and metformin, and sulphonylurea and metformin.

To find out the progression to insulin use by year, the physicians used the Cox proportional hazards regression model.

How well do you really know your competitors?

Access the most comprehensive Company Profiles on the market, powered by GlobalData. Save hours of research. Gain competitive edge.

Company Profile – free sample

Thank you!

Your download email will arrive shortly

Not ready to buy yet? Download a free sample

We are confident about the unique quality of our Company Profiles. However, we want you to make the most beneficial decision for your business, so we offer a free sample that you can download by submitting the below form

By GlobalData
Visit our Privacy Policy for more information about our services, how we may use, process and share your personal data, including information of your rights in respect of your personal data and how you can unsubscribe from future marketing communications. Our services are intended for corporate subscribers and you warrant that the email address submitted is your corporate email address.

However, the study had number of limitations including unavailability of data for day-of-supply for prescription and stopping dates of medications, no clear information regarding whether patient took medications as per the physician’s prescription, amongst others.

Merck said in a statement: "Due to the methods employed in this analysis, the time period in which an outcome can be observed must be prespecified and patients without complete data needed to be excluded."