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For the third time in two years, FDA approves weight loss pill

For the third time in two years, the Food and Drug Administration approves a new weight-loss pill

By Heather Records

WASHINGTON, Sept. 11 (UPI) -- On Wednesday, the FDA approved a new weight-loss pill.

The pill--called Contrave-- made by Orexigen Therapeutics Inc., San Diego, and will be marketed by Takeda Pharmaceutical of Japan.

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It joins two pills already on the market to help adults fight their weight, Qsymia and Belviq.

In a press release, the FDA said Contrave is approved for adults with a BMI of 30 or higher or adults with a BMI of 27 or greater. They must also have at least one weight-related condition like high blood pressure, type 2 diabetes or high cholesterol.

The FDA's Jean-Marc Guettier also said, "When used as directed in combination with a healthy lifestyle that includes a reduced-calorie diet and exercise, Contrave provides another treatment option for chronic weight management for people who are obese or are overweight and have at least one weight-related health condition."

Contrave is a combination of two drugs--already approved by the FDA--naltrexone and bupropion. Naltrexone is approved to treat alcohol and opioid dependence. Bupropion is approved to treat depression and seasonal affective disorder and as an aid to smoking cessation treatment.

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