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FDA panel recommends approval of obesity drug
Published October 27, 2015
** ADVANCE FOR SUNDAY, SEPT. 28 ** Angel Moreno, 14, who weighs 71.5 kg, or 156.528 lb, gets a check-up at Mexico's Children's Hospital in Mexico City, Friday, Aug. 29, 2008. Mexico is on track to surpass the United States as one of the world's fattest countries by 2018. Nearly half of Mexico's 110 million people already are overweight, while the number of fat children has climbed 8 percent a year in the last decade. (AP Photo/Alexandre Meneghini) (AP)
A Food and Drug Administration (FDA) advisory committee recommended Thursday the agency approve a new drug to treat obesity, the second time this year agency advisers have backed a fat-fighting medication.
Arena Pharmaceuticals Inc. makes the drug, lorcaserin, and hopes to market it under the brand name Lorqess.
The advisory committee voted 18-4, with one abstention, that the weight loss benefits of the medication outweigh any possible risk.
Research showed signs the medicine might be linked to a small risk of cancer and heart valve disease.
In February, an advisory committee recommended the agency approve Vivus Inc.'s Qnexa drug for weight loss. The agency has not acted on it yet.
Lorcaserin was rejected in 2010 by the federal agency, which cited "modest weight loss" and concerns about a study that linked the drug to mammary tumors in rats.
This time, Arena returned to the FDA with new data showing that 38 percent of patients on the drug had weight loss of five percent or more in a year, compared with 16 percent of patients on a placebo.
Overall, neither Arena nor the FDA officials who testified presented data that were definitive about safety concerns.
William R. Shanahan Jr., a senior vice president at Arena, contended the cancer effect was "rat-specific," not likely meaningful in humans, and that evidence "mitigates human risk."
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