1:37 p.m.
Diabetics gained a new way of controlling their blood sugar levels today with federal approval of a novel pill for type 2 diabetes, which affects about 20 million Americans.
The Food and Drug Administration said it approved Januvia, which enhances the body’s ability to reduce its blood sugar levels, after clinical trials showed the new pill works just as well as older diabetes drugs but with fewer side effects, such as weight gain. The drug is made by Merck & Co. Inc.
Merck is expected to charge $4.86 for the once-daily tablet, a price that may limit its use. Older diabetes drugs can cost 50 cents a day.
Januvia, also known as sitagliptin phosphate, works with a one-two punch: It increases levels of a hormone that triggers the pancreas to produce more insulin to process blood sugar while simultaneously signaling the liver to quit making glucose. The pill does that by blocking production of an enzyme, called DPP-4, that normally inactivates that hormone.
Januvia is unlike any other oral drug for treating type 2 diabetes. However, Novartis AG hopes to win FDA approval for a similar drug later this year.
In type 2 diabetes, patients either don’t produce enough insulin or cells in the body ignore it. Insulin is needed to process sugar. Without it, blood sugar levels soar.
The FDA approved Januvia for use in addition to diet and exercise to improve blood sugar levels in patients with type 2 diabetes, alone or in combination with other commonly prescribed drugs.
“For the millions of Americans with type 2 diabetes, who continue to have inadequate blood sugar control, the approval of Januvia marks an important advance in the fight against diabetes,” said Steven Galson, director of FDA’s Center for Drug Evaluation and Research. “We now have another new option that treats the disease in an entirely new way that can be added to existing treatment regimens to help patients gain more control over their blood sugar levels.”
American Diabetes Association guidelines suggest that diabetics cut their levels of an averaged measure of blood sugar levels, called A1c, to less than 7 percent. Many, if not most, diabetics exceed that threshold. Helping them drop below it could reduce their risk of serious complications, including kidney failure and amputations, the diabetes group says.
At a diabetes conference in June, Merck said Januvia lowered blood sugar levels by 0.67 percent in a yearlong trial, or just as much as another, older drug, glipizide. Roughly two-thirds of patients reached the ADA’s 7 percent goal.
Most important, Merck said the Januvia patients also lost weight and experienced fewer episodes of exceedingly low blood sugar than those on glipizide, a member of the sulfonylurea class of drugs. Excess weight is a common problem in type 2 patients.
The most common side effects of Januvia in clinical studies were upper respiratory tract infection, sore throat and diarrhea, the FDA said.
Analysts have predicted Januvia sales could reach $1 billion in 2009 for Merck, based in Whitehouse Station, N.J.
Merck hopes to win FDA approval in late March for another pill, called MK-0431, that combines Januvia and the diabetes drug metformin.
“There is a huge need for additional therapeutic options in this marketplace,” said Jay Galeota, who manages Merck’s global diabetes drug business.
More than 230 million people worldwide have diabetes, up from just 30 million in 1985, according to the International Diabetes Federation. Diabetes is expected to affect 350 million people by 2025.
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