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发表于 2002-10-20 00:39
Triangle制药公司的核苷类似物Coviracil(FTC, emtricitabine~恩曲他滨/鸟环核苷)两年来临床试验结果显示能降低慢性感染病人的乙肝病毒水平并抗药性小...
Coviracil Is an Effective HBV Therapy with Low Resistance Rates Following 2 Years of Therapy
By Brian Boyle, MD
Hepatitis B virus (HBV) infection is both a common and potentially fatal viral infection. Effective treatment options for this condition have been limited to this point; however, the number of effective agents for the treatment of this condition has steadily grown over the past few years.
Some exciting drugs in the pipeline are moving through clinical trials and one of these drugs, Coviracil (emtricitabine, FTC) is a nucleoside analogue (NA) that has potent activity against HBV and HIV. While Coviracil has a resistance profile similar to Epivir (lamivudine, 3TC), preliminary data from a study evaluating Coviracil in patients with chronic HBV indicated that it is very effective treatment of HBV and that there was a low rate of resistance development. Further follow-up of this study was presented at the 42nd ICAAC.
The Study, FTCB-102, is a randomized, double-blind, dose ranging trial comparing 3 once-daily doses (25, 100, 200mg) of FTC for 1 year in 98 patients. After 1 year of therapy, all patients were switched to a 200mg once-daily dose of Coviracil.
Using an Intent-to-Treat analysis, after 2 years of treatment with Coviracil, 42% of the patients had undetectable HBV levels, 76% had normalized their ALT levels, 51% had seroconverted to HBeAg negative and 29% to HBeAb positive. The patients who received 200mg of Coviracil for 2 years had a lower rate of Coviracil resistance (19%) than patients who received 25 or 100mg for the first year followed by 200mg (20% and 37% respectively). The Coviracil therapy was extremely well tolerated.
The authors conclude, "[Coviracil] produced a sustained virologic and serologic response (29% HBeAg conversion). At 2 years the incidence of mutations was low (19%) among the patients receiving 200mg for the duration of the study, suggesting that potent viral suppression limits the emergence of resistant variants. These data are consistent with an HIV clinical trial, regarding the rate of developing the M184V mutation."
10/14/02
Reference
H Mommeja Marin and others. Antiviral Activity and Incidence of Resistance after Treatment for Two Years with Emtricitabine in Patients with Chronic Hepatitis B. Abstract V-239. 42nd ICAAC. September 27-30, 2002. San Diego, CA. (Hepatitis.com, 42nd ICCAAC Summary)
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