Scientists announced today that a new type of contraceptive gel that is also designed to protect against sexually transmitted infections will be the first of its kind to begin clinical efficacy trials at the National Institutes of Health's Contraceptive Clinical Trials Network.
The gel, known by the brand name BufferGelTM, was jointly developed by researchers at The Johns Hopkins University and the private firm ReProtect LLC. The new trial will test whether women using BufferGel and a diaphragm can reduce the risk of pregnancy as effectively as women using a conventional spermicidal detergent and a diaphragm.
BufferGel is applied vaginally before sex, like conventional spermicides. Unlike these spermicides, which use detergents to kill sperm, BufferGel contains no soaps. Developers deliberately avoided including soaps or detergents because they can irritate the vaginal lining after frequent use.
"The normal acidity levels in the vagina can readily kill sperm and many of the germs that cause sexually transmitted infections," explains Cone, who is also managing director of ReProtect. "That's why your stomach's contents are acidic. Most germs just don't survive long in acidic environments."
Semen eliminates vaginal acidity for several hours to allow sperm to leave the vagina and enter the uterus. Unfortunately, this also can help make it possible for germs to infect the sexual partner. Cone says BufferGel should block this effect, killing both sperm and germs by rapidly acidifying semen.
While reinforcing the vagina's natural acidity seemed like a simple enough approach for developing a contraceptive microbicide, several practical considerations made developing a useful compound challenging, according to Cone.
"Not only must the compound kill both sperm and germs, it must do so without hurting the friendly bacteria in a healthy vagina, like the lactobacilli," he explains. "Also, it mustn't smell bad or taste bad or stain the sheets. And most importantly, it mustn't irritate sensitive vaginal tissues."
BufferGel has met those standards both in animal trials and in extensive clinical safety trials, according to Cone.
For the new contraceptive efficacy trial, researchers at 10 sites in the United States are enrolling 1,000 women. Participants in the study must be in a sexually active and monogamous relationship and at low risk for infection by sexually transmitted diseases. They must agree not to use other forms of contraception beyond that supplied by the study, and be willing to risk getting pregnant. Study participants will use a diaphragm with either BufferGel or a conventional spermicide.
"In this trial, we want to achieve the highest possible level of protection," says Thomas Moench, medical director for ReProtect LLC. "We're including a diaphragm because it places a discrete physical barrier over the cervix, significantly enhancing the protective actions of contraceptive microbicides."
Moench, formerly an assistant professor of infectious diseases at the Johns Hopkins Medical Institutions, originally created BufferGel with Cone. Hopkins and ReProtect LLC are developing BufferGel through a cooperative research agreement.
Researchers are also currently planning a larger trial to test BufferGel's ability to block transmission of HIV and genital herpes. The trial is scheduled to take place through NIH's HIV Prevention Trials Network next year.
Cone is a part-owner of ReProtect. His financial interests in this research are being managed by the Johns Hopkins University in accordance with its conflict-of- interest policies. NIH is funding the trials.
Go to Headlines@HopkinsHome Page