Population Pharmacokinetics of Tebipenem Pivoxil (ME1211), a Novel Oral Carbapenem Antibiotic, in Pediatric Patients with Otolaryngological Infection or Pneumonia

• Published in: Drug metabolism and pharmacokinetics 2008-01, Vol.23 (6), p.434-446
• Main Authors: Sato, Nobuo, Kijima, Koji, Koresawa, Tomokazu, Mitomi, Nayu, Morita, Jun, Suzuki, Hisashi, Hayashi, Hiroyuki, Shibasaki, Shigeki, Kurosawa, Tohru, Totsuka, Kyoichi
• Format: Article
• Language: English
• Subjects: Administration, Oral; Adolescent; bacterial pneumonia; Carbapenems - administration & dosage; Carbapenems - pharmacokinetics; Child; Child, Preschool; Female; H. influenzae; Humans; Infant; Male; oral carbapenem; otolaryngological infection; Otorhinolaryngologic Diseases - drug therapy; Otorhinolaryngologic Diseases - metabolism; pediatric patients; penicillin-resistant S.pneumoniae (PRSP); Pneumonia, Pneumococcal - drug therapy; Pneumonia, Pneumococcal - metabolism; Population; population pharmacokinetics; tebipenem pivoxil (TBPM-PI, ME1211)
• ISSN: 1347-4367; 1880-0920
• DOI: 10.2133/dmpk.23.434

Tebipenem pivoxil (TBPM-PI, ME1211) has been under development as the world's first oral carbapenem for treatment of otolaryngological/respiratory infections caused by drug-resistant S. pneumoniae in pediatric patients. In order to treat these infections effectively, it is important to design optimal dosing regimens based on the pharmacokinetics/pharmacodynamics (PK/PD) relationships, which can be characterized by clarifying the pharmacokinetics of tebipenem (TBPM) in the pediatric population. We therefore performed an population pharmacokinetic analysis using plasma TBPM concentrations obtained from pediatric patients with otolaryngological infection or bacterial pneumonia (0.5-16 years old; n = 217, 395 points), after repeated oral administration of TBPM-PI at a dose of 4 or 6 mg/kg b.i.d. A one-compartment model with first-order absorption was adopted. In analysis, weight-normalized creatinine clearance (Ccr) and age were the most significant covariates that respectively explained inter-subject variability in weight-normalized apparent clearance (CL/F) and volume of distribution (Vd/F) of TBPM. The CL/F of TBPM increased with Ccr, and the Vd/F decreased with age. Based on the results of the present analysis, validity of the presently recommended dosage regimen of TBPM-PI in pediatric patients is discussed.