ALACHUA, Fla. -
Oragenics Inc. plans to start human safety studies of
its replacement therapy early next year, using a
genetically modified bacteria to battle decay caused
by naturally occurring microbes already in the mouth.
The Food and Drug
Administration (FDA) on Tuesday lifted a clinical
hold on the tooth decay treatment.
In a press release
Tuesday, the Alachua, Fla.-based biotechnology
company said the FDA (news - web sites) approved a
Phase I trial after reviewing the study's clinical
design.
"The idea is simply to
use good bacteria to fight bad bacteria," Oragenics'
chief scientific officer, Jeffrey D. Hillman, told
The New York Times for a story in Tuesday's editions.
In May 2003, the FDA
placed Replacement Therapy's Investigational New Drug
application on clinical hold pending a review of the
study's design. In March, an FDA advisory committee
recommended that the trial should be carried out
under the protocol proposed by Oragenics.
The first trial will
involve 15 volunteers wearing dentures, to test the
procedure's safety, the newspaper reported.
Eventually, the trials will help determine if the
bacteria is effective against fighting cavities.
Replacement Therapy
treats dental caries, which is the demineralization
of a tooth's surface caused by bacteria.