Wednesday, August 31, 2011

Experimental Obesity Drug Beats Placebo Again



The experimental weight loss drug lorcaserin may spur modest weight loss without the heart risks of some older drugs, a new clinical trial confirms though whether the medication will ever reach the market remains up in the air.

Last October, the U.S. Food and Drug Administration (FDA) declined to approve lorcaserin as an obesity treatment, citing research in rats that suggested there could be a cancer risk.

This latest study, reported in the Journal of Clinical Endocrinology and Metabolism, backs up earlier research showing that lorcaserin can shave off some extra pounds.

Of 4,000 obese adults who used the drug for a year, more than 40 percent lost at least five percent of their initial weight versus a quarter of those given placebo pills who lost that much.

And the drug facilitated weight loss without raising the risk of heart-valve damage, according to the findings.

Reports of fatal heart-valve problems are what caused the infamous diet drug known as “fen-phen” to be pulled from the market in 1997.

Still, it’s unclear whether lorcaserin will ultimately play any role in the battle against obesity, which now affects about one third of U.S. adults.

The drug’s maker, Arena Pharmaceuticals Inc, has said it will conduct further research into the potential cancer risk. Arena’s new drug application to the FDA is still considered “open” while the company gathers data to answer the agency’s remaining questions about lorcaserin.

Drugmakers have struggled for years to develop weight-loss drugs that are both effective and safe.

Like fen-phen before it, another diet drug Meridia was pulled from the U.S. market last year after being linked to heart problems in some users.

And lorcaserin is one of three experimental obesity drugs rejected by the FDA in the past year over safety concerns. The other two are Orexigen Therapeutics’ Contrave, which combines the antidepressant bupropion with naltrexone, a drug used to fight alcohol and drug addiction; and Vivus Inc’s Qnexa, a combination of the appetite suppressant phentermine and the anti-seizure drug topiramate.

Continue Reading at Manila Bulletin