TY - JOUR
T1 - Basic and clinical studies on T-3262 in urology
AU - Tsugawa, Masaya
AU - Yamada, Daisuke
AU - Nasu, Yoshitsugu
AU - Kishi, Mikio
AU - Kumon, Hiromi
AU - Ohmori, Hiroyuki
AU - Nanba, Katsuichi
AU - Kondo, Katsuyoshi
AU - Katayama, Yasuhiro
AU - Akaeda, Teruaki
AU - Akazawa, Nobuyuki
PY - 1988/1/1
Y1 - 1988/1/1
N2 - T-3262, a new pyridone-carboxylic acid, was evaluated basically and clinically in the urological field. 1) Minimal inhibitory concentrations (MICs) of T-3262 were compared with those of norfloxacin, ofloxacin and ciprofloxacin using 189 clinical isolates from urinary tract infections (UTI). The antibacterial activity of T-3262 was as high as or even higher than those of the three other drugs against all species studied. 2) The concentration of T-3262 in the prostate after oral administration of 150 mg was studied. The concentration in the prostatic tissue, 2 and 4 hours after administration, was 0.120±0.075 μg/g (mean ± SE) and 0.245±0.079 μg/g, respectively. Similarly, the concentration in the prostatic fluid, 1, 2 and 4 hours after administration, was O.047±0.014 μg/ml, 0.111±0.080 μg/ml and 0.033±0.014 μg/ml, respectivery. 3) Forty-one patients with UTI were treated by oral administration of T-3262 at a dosage of 75 or 150 mg two or three times daily for 3-14 days. According to the criteria of the Japanese UTI Committee, the overall clinical efficacy rate was 100%(5/5) in acute uncomplicated cystitis and 60.0%(15/25) in complicated UTI. 4) No drug-related side effects, including abnormal laboratory findings, were observed in any of the 40 cases.
AB - T-3262, a new pyridone-carboxylic acid, was evaluated basically and clinically in the urological field. 1) Minimal inhibitory concentrations (MICs) of T-3262 were compared with those of norfloxacin, ofloxacin and ciprofloxacin using 189 clinical isolates from urinary tract infections (UTI). The antibacterial activity of T-3262 was as high as or even higher than those of the three other drugs against all species studied. 2) The concentration of T-3262 in the prostate after oral administration of 150 mg was studied. The concentration in the prostatic tissue, 2 and 4 hours after administration, was 0.120±0.075 μg/g (mean ± SE) and 0.245±0.079 μg/g, respectively. Similarly, the concentration in the prostatic fluid, 1, 2 and 4 hours after administration, was O.047±0.014 μg/ml, 0.111±0.080 μg/ml and 0.033±0.014 μg/ml, respectivery. 3) Forty-one patients with UTI were treated by oral administration of T-3262 at a dosage of 75 or 150 mg two or three times daily for 3-14 days. According to the criteria of the Japanese UTI Committee, the overall clinical efficacy rate was 100%(5/5) in acute uncomplicated cystitis and 60.0%(15/25) in complicated UTI. 4) No drug-related side effects, including abnormal laboratory findings, were observed in any of the 40 cases.
UR - http://www.scopus.com/inward/record.url?scp=0024230582&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=0024230582&partnerID=8YFLogxK
U2 - 10.11250/chemotherapy1953.36.Supplement9-Clinical_1074
DO - 10.11250/chemotherapy1953.36.Supplement9-Clinical_1074
M3 - Article
AN - SCOPUS:0024230582
SN - 0009-3165
VL - 36
SP - 1074
EP - 1090
JO - Chemotherapy
JF - Chemotherapy
ER -