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PK/PD of Cefadroxil in Staphylococcus Aureus Bacteremia, a preliminary study

Status
Not yet recruiting
Phases
Phase 2
Study type
Interventional
Source
EU CTIS
Registry ID
CTIS2025-522547-17-00
Enrollment
25
Registered
2025-09-24
Start date
Unknown
Completion date
Unknown
Last updated
2025-09-24

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

staphylococcus aureus bacteremia

Brief summary

PK Assessment: Establishment of correct cefadroxil doses through Monte Carlo simulations (serum concentrations > MIC for at least 50% of the day). PD Assessment: Therapeutic failure will be assessed as a composite endpoint of relapsing SAB, deep-seated infection with the same bacteria, switch to another antimicrobial regimen due to ad-verse events or failure to improve, attributable rehospitalization, or attributable mortality within 90 days of inclusion. Adverse Events (AE): Monitoring and re

Interventions

DRUGCefadroxil Sandoz 500 mg harde capsules

Sponsors

UZ Brussel
Lead SponsorOTHER

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Design outcomes

Primary

MeasureTime frame
PK Assessment: Establishment of correct cefadroxil doses through Monte Carlo simulations (serum concentrations > MIC for at least 50% of the day). PD Assessment: Therapeutic failure will be assessed as a composite endpoint of relapsing SAB, deep-seated infection with the same bacteria, switch to another antimicrobial regimen due to ad-verse events or failure to improve, attributable rehospitalization, or attributable mortality within 90 days of inclusion. Adverse Events (AE): Monitoring and re

Countries

Belgium

Outcome results

None listed

Source: EU CTIS · Data processed: Feb 4, 2026