TY - JOUR KW - Animals KW - Anti-Bacterial Agents KW - Anti-Infective Agents KW - Aza Compounds KW - Disease Models, Animal KW - Dose-Response Relationship, Drug KW - Drug Therapy, Combination KW - Female KW - Fluoroquinolones KW - Leprostatic Agents KW - leprosy KW - Mice KW - Mice, Inbred Strains KW - Minocycline KW - Moxifloxacin KW - Probability KW - Quinolines KW - Rifampin KW - Treatment Outcome AU - Ji B AU - Grosset J AB -

To further the development of a multidrug regimen for treatment of leprosy that is suitable for monthly administration and fully supervisable, the bactericidal activities against Mycobacterium leprae of HMR 3647 (HMR), moxifloxacin (MXFX) and rifapentine (RPT) were measured by the proportional bactericide technique in the mouse footpad system, and compared with those of the established antileprosy drugs clarithromycin (CLARI), ofloxacin (OFLO) and rifampicin (RMP). Administered in five daily doses of 100 mg per kg body weight, HMR appeared slightly more bactericidal than CLARI, but the difference did not attain statistical significance. Administered as single doses, MXFX in a dosage of 150 mg per kg was more active than OFLO in the same dosage, and displayed the same level of activity as RMP in a dosage of 10 mg per kg; the combination MXFX-minocycline (MINO) (MM) was more bactericidal than the combination OFLO-MINO (OM); RPT in a dosage of 10 mg per kg was more bactericidal than RMP administered in the same dosage, and even more active than the combination RMP-OFLO-MINO (ROM); the combination RPT-MXFX-MINO (PMM) killed 99.9% of viable M. leprae, and was slightly more bactericidal than was RPT alone, indicating that the combination PMM showed an additive effect against M. leprae. These promising results justify a clinical trial among lepromatous patients, in which MM is being compared with OM, and PMM with ROM, in terms of efficacy and tolerance.

BT - Leprosy review C1 - http://www.ncbi.nlm.nih.gov/pubmed/11201894?dopt=Abstract CN - Infolep Library - available DA - 2000 Dec DO - 10.5935/0305-7518.20000074 J2 - Lepr Rev LA - eng N2 -

To further the development of a multidrug regimen for treatment of leprosy that is suitable for monthly administration and fully supervisable, the bactericidal activities against Mycobacterium leprae of HMR 3647 (HMR), moxifloxacin (MXFX) and rifapentine (RPT) were measured by the proportional bactericide technique in the mouse footpad system, and compared with those of the established antileprosy drugs clarithromycin (CLARI), ofloxacin (OFLO) and rifampicin (RMP). Administered in five daily doses of 100 mg per kg body weight, HMR appeared slightly more bactericidal than CLARI, but the difference did not attain statistical significance. Administered as single doses, MXFX in a dosage of 150 mg per kg was more active than OFLO in the same dosage, and displayed the same level of activity as RMP in a dosage of 10 mg per kg; the combination MXFX-minocycline (MINO) (MM) was more bactericidal than the combination OFLO-MINO (OM); RPT in a dosage of 10 mg per kg was more bactericidal than RMP administered in the same dosage, and even more active than the combination RMP-OFLO-MINO (ROM); the combination RPT-MXFX-MINO (PMM) killed 99.9% of viable M. leprae, and was slightly more bactericidal than was RPT alone, indicating that the combination PMM showed an additive effect against M. leprae. These promising results justify a clinical trial among lepromatous patients, in which MM is being compared with OM, and PMM with ROM, in terms of efficacy and tolerance.

PY - 2000 SP - S81 EP - 7 T2 - Leprosy review TI - Combination of rifapentine-moxifloxacin-minocycline (PMM) for the treatment of leprosy. UR - http://leprev.ilsl.br/pdfs/2000/v71s1/pdf/v71s1a17.pdf VL - 71 Suppl SN - 0305-7518 ER -