June 11, 2001
"That's unprecedented," said William J. Burman, an infectious disease specialist at the Denver Medical Health Center. "Rifampin's king, and I don't know whether even a quinolone could dethrone it," Burman conjectured, but "if something like the Chennai trials could be repeated here, does that mean we could increase two-month conversion rates by 10 percent?" If that were the case, quinolones might lead to shorter therapy or could serve in regimens entailing markedly less frequent therapy.
Researchers at the Tuberculosis Trials Consortium (TBTC) want to team a quinolone with rifapentine (RFP), the drug with the long half-life approved in 1998 for TB treatment. The TBTC is the investigator-led collaboration funded by the CDC. Rick O'Brien, MD, head of the research and evaluation branch of the CDC's Division of TB Elimination, thinks it might be possible to use quinolone along with RFP to achieve a super-short induction phase of perhaps two weeks, followed by once-weekly therapy for six months.
Ofloxacin along with a quinolone known as levofloxacin are well-respected members of second-line drugs used to treat drug-resistant disease. There are plenty of safety data on levofloxacin; however, data are scanty for long-term use of most other quinolones. According to Burman, "We've tried telling the FDA and the drug companies how we use quinolone in TB treatment all the time for long-term treatment," he said, "but they say they're still worried about side effects, and that they need more data."
The first work of the TBTC will likely be a small Phase II safety and tolerability trial that looks at two-month conversion rates. The other challenge ahead is which quinolone to use. The final hurdle is money. "If we don't get more of it, we won't be doing any trials at all on quinolones this year," said Burman.
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