Individualized Precision Therapy With Ceftobiprole Guided by PK/PD in Geriatric Populations

ConditionCeftobiprole
Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age60+
SponsorChinese PLA General Hospital

About this trial

Ceftobiprole, a fifth-generation cephalosporin, exhibits potent antibacterial activity against MRSA, penicillin-resistant Streptococcus pneumoniae (PRSP), and certain Gram-negative bacteria (e.g., Pseudomonas aeruginosa). In elderly patients, significant interindividual variability often leads to inappropriate dosing (subtherapeutic or excessive), compromising efficacy or increasing toxicity risks. This prospective, multicenter study will enroll patients aged ≥60 years receiving ceftobiprole. Using LC-MS/MS for therapeutic drug monitoring (TDM), we will measure plasma concentrations and integrate individual characteristics (age, body weight, creatinine clearance, etc.). Population pharmacokinetic (PPK) modeling with Bayesian forecasting will be employed to estimate individual PK parameters and identify covariates influencing variability, thereby establishing a PPK model for ceftobiprole in the elderly.

Based on pathogen-specific MIC values, dosing regimens (dose, frequency) will be dynamically optimized to guide precision therapy. Subsequent TDM data will continuously refine the PPK model, creating a self-optimizing system. This framework lays the groundwork for extending individualized treatment strategies to other antimicrobials in geriatric populations.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Aged ≥60 years Scheduled to receive ceftobiprole therapy for >5 days No prior ceftobiprole use within 1 month before enrollment

Disqualifiers

Patients requiring renal replacement therapy (hemodialysis, peritoneal dialysis, or continuous renal replacement therapy [CRRT]) or with renal impairment history (nephrectomy, renal transplantation, solitary kidney, uremia) Obese patients with body mass index (BMI) ≥30 kg/m²

Trial population

Professional Translation for Clinical Research Protocols: Enroll patients aged ≥60 years receiving ceftobiprole therapy at Chinese PLA General Hospital

Trial design

Design model

Cohort

Time perspective

Prospective

Treatments tested in this trial

  • LS/MS

    Diagnostic test

    Quantitative determination of ceftobiprole concentrations in plasma and urine was performed using liquid chromatography-tandem mass spectrometry (LC-MS/MS).

Treatment groups

150 Participants
are divided into 1 treatment group
Group A: Ceftobiprole1 intervention

Trial outcomes

Primary outcomes

1

Ceftobiprole Concentration

Plasma Ceftobiprole Concentration and Urinary Ceftobiprole Concentration

Time frame
after 3 days of antibiotic therapy

Secondary outcomes

Other outcomes

Sponsors and contacts

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