Experimental Drug Achieves Unprecedented Weight Loss
An investigational combination of drugs already approved to treat obesity, migraine, and epilepsy produced up to a 10 percent weight loss in obese individuals participating in a one-year clinical trial, according to researchers at Duke University Medical Center.
Appearing online in The Lancet today, the study found that treatment with the controlled-release combination therapy consisting of phentermine and topiramate also achieved significant reductions in blood pressure and hemoglobin A1C.
Study participants also experienced improvements in cholesterol, triglycerides and inflammatory markers, including C-reactive protein, when taking either of two doses of the combination when compared to placebo.
"Patients receiving this combination experienced 8.6 percent greater weight loss, on average, compared to those patients receiving placebo," says Kishore M. Gadde, MD, director of Duke's obesity clinical trials program.
"This kind of weight loss, coupled with significant reductions in cardiometabolic risk factors represents a potentially important advancement in the management of obesity."
Currently, orlistat is the only drug available for the long-term treatment of obesity. It is marketed in prescription strength as Xenical, and available over the counter as Alli.
Meta-analysis studies have shown that treatment with orlistat, at maximum strength, can lead to approximately seven-pound greater weight loss compared to treatment with placebo after one year. "The combination drug achieves about 19 pounds of weight loss relative to placebo at one year," Gadde says.
The 56-week, phase three study was conducted in 93 U.S. centers with 2,487 patients who had a BMI of 27-45kg/m2, and two or more co-morbidities such as diabetes or heart disease. Patients were randomly assigned to receive either a placebo or one of two low-dose drug combinations.
The study tested phentermine, a short-term obesity treatment available since 1959, and topiramate, marketed under the trade name Topamax, in doses up to 400mg to treat epilepsy and prevent migraines. Patients in the study also received diet and exercise advice.
The study was funded by Vivus, which is seeking FDA approval to market the combination therapy under the trade name Qnexa. In October 2010, the FDA ruled that the New Drug Application could not be approved in its current form, and asked the company for more safety data.
In March, the FDA issued a warning regarding the use of topiramate during pregnancy, stating that pregnant women who take the drug are at considerably increased risk of having babies born with cleft lip and/or cleft palate. Topiramate has also been associated with memory problems and mood changes, including depression and anxiety.
Gadde says 34 women became pregnant while in Qnexa clinical trials, and "no birth defects were reported for the babies born." Even so, Gadde says pregnant women would not be candidates for use of this drug because "there is no reason for women to use weight loss drugs while they are pregnant or trying to become pregnant."
The study used once-daily oral doses of the combined drugs. Phentermine 7.5mg plus topiramate CR 46mg achieved 7.8 percent weight loss (p<0.0001 vs placebo). Phentermine 15mg plus topiramate CR 92mg achieved 9.8 percent weight loss (p<0.0001 vs placebo). The placebo group experienced 1.2 percent weight loss.
The greatest improvement in cardiovascular disease and diabetes were seen in high risk patients among the groups given placebo, phentermine 7.5mg plus topiramate 40mg, or phentermine 15mg plus topiramate 92mg respectively:
- Systolic blood pressure: -4.9mmHg, -6.9mmHg, -9.1mmHg
- Diastolic blood pressure: -3.9mmHg, -5.2mmHg, -5.8mmHg
- Total cholesterol: -4.9 percent, -5.7 percent, -7.8 percent
- LDL: -3.6 percent, 0.7 percent, -4.3 percent
- HDL: 2.8 percent, 9.5 percent, 10.7 percent
- Triglycerides: -8.8 percent, -24.1 percent, -25.6 percent
- Hemoglobin A1C in diabetics: -0.1 percent, -0.4 percent, -0.4 percent
- Fasting insulin in pre-diabetics: 6.0pmol/L, -29.2pmol/L, -31.9pmol/L
The most common adverse events in the groups given placebo, phentermine 7.5mg plus topiramate 40mg, or phentermine 15mg plus topiramate 92mg, respectively were:
- Dry mouth: 2 percent, 13 percent, 21 percent
- Parethesia (numbness or tingling): 2 percent, 14 percent, 21 percent
- Constipation: 6 percent, 15 percent, 17 percent
- Insomnia: 5 percent, 6 percent, 10 percent
- Dizziness: 3 percent, 7 percent, 10 percent
- Dysgeusia (distorted sense of taste): 1 percent, 7 percent, 10 percent
Depression-related events were found in 4 percent assigned to placebo, 4 percent assigned to phentermine 7.5mg plus topiramate 46mg, and 7 percent to phentermine 15mg plus topiramate 92mg. Anxiety-related events were reported in 3 percent, 5 percent, and 8 percent respectively.
"Although the overall incidence of these events was relatively small," Gadde says, "clearly there is a dose-related increase in risk."
The drug combination works in two ways, he says. Phentermine increases the release of norepinephrine, a brain chemical that may influence hunger and satiety. Topiramate has numerous mechanisms of action including effects on sodium channels, glutamate and GABA transmission, and carbonic anhydrase inhibition, although the mechanism responsible for weight loss is not clearly known.
"We believe it mainly works by reducing hunger and increasing satiety, but may have an independent effect on glucose control," Gadde says.
"More patients on placebo developed diabetes during one year than patients who were on the combination drug. More patients on the combination drug were also able to go off their diabetes and blood pressure medicines."
Gadde believes more treatments are needed for obesity as rates increase. "Two-thirds of Americans are overweight or obese. For obese patients who have failed to achieve meaningful weight loss with diet and exercise, we have just one treatment before jumping to bariatric surgery. We need more treatment options."
Dr. Gadde has received funding from Vivus for conduct of research studies. He was a paid consultant to Vivus until 2008.