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A Study of Ceftobiprole Compared With Standard Antibiotic Treatment in Children With Staphylococcus Aureus Bacteremia (SAB) Infection, Including Right-sided Heart Infection

4. november 2026 oppdatert av: ISTx, LLC

A Multicenter, Randomized, Investigator-blind, Active-controlled Study to Evaluate the Safety, Tolerability, Efficacy, and Pharmacokinetics of Ceftobiprole Versus Standard-of-care Treatment in Pediatric Patients From Birth to Less Than 18 Years With Staphylococcus Aureus Bacteremia, Including Right-sided Infective Endocarditis

This clinical trial will evaluate the safety, and effectiveness of ceftobiprole compared to standard-of-care antibiotic treatment in children from birth to less than 18 years of age with Staphylococcus aureus bloodstream infection, including right-sided infective endocarditis (IE). The trial will also evaluate the pharmacokinetics of ceftobiprole.

Studieoversikt

Studietype

Intervensjonell

Registrering (Antatt)

60

Fase

  • Fase 3

Kontakter og plasseringer

Denne delen inneholder kontaktinformasjon for de som utfører studien, og informasjon om hvor denne studien blir utført.

Studiekontakt

Deltakelseskriterier

Forskere ser etter personer som passer til en bestemt beskrivelse, kalt kvalifikasjonskriterier. Noen eksempler på disse kriteriene er en persons generelle helsetilstand eller tidligere behandlinger.

Kvalifikasjonskriterier

Alder som er kvalifisert for studier

3 dager til 17 år (Barn)

Tar imot friske frivillige

Nei

Kjønn som er kvalifisert for studier

Alle

Beskrivelse

Key Inclusion Criteria:

  • Pediatric age from birth to < 18 years old, with body weight ≥ 3.7 kg at the time of consent. Participants in the birth to < 2-year-old cohort should have a gestational age ≥ 37 weeks and postnatal age ≥ 3 days

  • Parent(s) or legal guardian(s) have provided documented informed consent, and participant has provided assent as per local standards.

  • SAB:

    1. Based on at least one blood culture obtained within 48 hours prior to randomization that is positive for S. aureus
    2. Persistent SAB

Key Exclusion Criteria:

  • Receipt of systemic antibacterial treatment for S. aureus infections exceeding 48 hours within the 7 days prior to randomization.
  • Infection with S. aureus known or suspected to be non-susceptible to ceftobiprole or available SOC comparator antibiotic options
  • Known concomitant bloodstream or non-bloodstream infections with Gram-negative bacteria at screening
  • Left-sided IE (known or suspected to be present at the time of randomization)
  • Contraindication to the administration of study treatments, including known clinically-relevant hypersensitivity to beta-lactam antibacterials
  • High probability of death within 7 days due to the underlying SAB or SAB-associated disease, or high probability of death within 28 days from an unrelated underlying disease
  • An absolute neutrophil count of < 0.5 x 10^9/L
  • Septic shock or hypotension unresponsive to IV fluids with or without vasopressors for ≥ 4 hours
  • SAB in participants with other foreign body material that cannot be removed within 7 days after randomization
  • Suspected or confirmed metastatic central nervous system S. aureus infection
  • Immunocompromising conditions
  • Receipt of systemic steroids (prednisolone ≥ 2 mg/kg per day, or equivalent) or immunosuppressive drugs within 2 weeks prior to screening
  • Any severe, acute or chronic medical or psychiatric condition, recent neurological event, or laboratory abnormality that may increase the risk associated with study participation or administration of study treatments, or may interfere with the interpretation of study results, and which, in the judgment of the Investigator, would make the participant inappropriate for entry into this study
  • eGFR of < 30 mL/min/1.73 m² for participants < 2 years old and < 15 mL/min/1.73 m² for participants ≥ 2 years old, or, for any age, requirement/anticipated requirement for plasmapheresis, peritoneal dialysis, hemodialysis, venovenous dialysis, continuous renal-replacement therapy (CRRT), or other forms of renal filtration.
  • History of seizures other than well-documented febrile seizures of childhood
  • Alanine transaminase (ALT) or aspartate transaminase (AST) levels > 5 × the upper limit of normal (ULN), OR total bilirubin > 2 × the ULN (except isolated unconjugated hyperbilirubinemia consistent with Gilbert's syndrome), OR severe hepatic disease classified as Child-Pugh class C

Studieplan

Denne delen gir detaljer om studieplanen, inkludert hvordan studien er utformet og hva studien måler.

Hvordan er studiet utformet?

Designdetaljer

  • Primært formål: Behandling
  • Tildeling: Randomisert
  • Intervensjonsmodell: Parallell tildeling
  • Masking: Enkelt

Våpen og intervensjoner

Deltakergruppe / Arm
Intervensjon / Behandling
Eksperimentell: Ceftobiprole

Participants randomized to this arm will receive intravenous (IV) ceftobiprole.

Ceftobiprole dosing is based on age/body weight and renal function and given at 7.5 mg/kg, 10 mg/kg, or 15 mg/kg (equivalent to 10 mg/kg, 13.3 mg/kg, or 20 mg/kg respectively of ceftobiprole medocaril sodium) q8h, q12h or q24h up to a maximum of 500 mg (equivalent to 667 mg of ceftobiprole medocaril sodium), with all doses infused over 2 hours.

Aktiv komparator: Standard-of-Care (SOC)

Participants randomized to this arm will receive intravenous (IV) standard-of-care (SOC) antibiotic treatment selected according to local guidelines or site-specific standard practice.

Dosage is per local product label based on the participant's age/body weight, and, if applicable, renal function.

Hva måler studien?

Primære resultatmål

Resultatmål
Tidsramme
Percentage of Participants with Treatment-Emergent Adverse Events (TEAEs)
Tidsramme: Day 1 through last follow-up (LFU) [up to 11 weeks]
Day 1 through last follow-up (LFU) [up to 11 weeks]
Percentage of participants with serious adverse events (SAEs)
Tidsramme: Baseline through LFU [up to 11 weeks]
Baseline through LFU [up to 11 weeks]
Percentage of participants with treatment-related adverse events (AEs)
Tidsramme: Day 1 through LFU [up to 11 weeks]
Day 1 through LFU [up to 11 weeks]
Percentage of participants with adverse events of special interest (AESIs)
Tidsramme: Baseline through LFU [up to 11 weeks]
Baseline through LFU [up to 11 weeks]
Percentage of participants with adverse events (AEs) leading to discontinuation of study-drug treatment
Tidsramme: Baseline through LFU [up to 11 weeks]
Baseline through LFU [up to 11 weeks]
Percentage of participants with treatment-emergent abnormal hematology laboratory test results
Tidsramme: Baseline through the end-of-treatment (EOT) visit [up to approximately 6 weeks]
Baseline through the end-of-treatment (EOT) visit [up to approximately 6 weeks]
Percentage of participants with treatment-emergent abnormal blood chemistry laboratory test results
Tidsramme: Baseline through the EOT visit [up to approximately 6 weeks]
Baseline through the EOT visit [up to approximately 6 weeks]
Percentage of participants with treatment-emergent abnormal urinalysis test results
Tidsramme: Baseline through the EOT visit [up to approximately 6 weeks]
Baseline through the EOT visit [up to approximately 6 weeks]
Change from baseline in body temperature
Tidsramme: Baseline through LFU visit [up to 11 weeks]
Baseline through LFU visit [up to 11 weeks]
Change from baseline in systolic blood pressure
Tidsramme: Baseline through LFU visit [up to 11 weeks]
Baseline through LFU visit [up to 11 weeks]
Change from baseline in diastolic blood pressure
Tidsramme: Baseline through LFU visit [up to 11 weeks]
Baseline through LFU visit [up to 11 weeks]
Change from baseline in respiratory rate
Tidsramme: Baseline through LFU visit [up to 11 weeks]
Baseline through LFU visit [up to 11 weeks]
Change from baseline in heart rate
Tidsramme: Baseline through LFU visit [up to 11 weeks]
Baseline through LFU visit [up to 11 weeks]

Sekundære resultatmål

Resultatmål
Tiltaksbeskrivelse
Tidsramme
Percentage of All-Cause Mortality (ACM)
Tidsramme: Through 28 days after EOT [up to approximately 10 weeks]

Defined as death from any cause including death due to SAB

Through 28 days after EOT [up to approximately 10 weeks]
Percentage of new metastatic foci or other complications of SAB
Tidsramme: Day 8 through test-of-cure (TOC) [up to approximately 8 Weeks]

Complications are considered new between Day 8 and TOC

Day 8 through test-of-cure (TOC) [up to approximately 8 Weeks]
Percentage of participants with Clinical Success at the TOC Visit
Tidsramme: TOC visit [7-14 days after EOT]

Success is defined as either cure or improvement

TOC visit [7-14 days after EOT]
Percentage of participants with Microbiological Success at the TOC Visit
Tidsramme: TOC visit (7-14 days after EOT)

Microbiological success is defined as eradication or presumed eradication.

TOC visit (7-14 days after EOT)
Percentage of participants with Overall Success at the TOC Visit
Tidsramme: TOC visit (7-14 days after EOT)

Overall success is defined as the achievement of both clinical success and microbiological success

TOC visit (7-14 days after EOT)
Ceftobiprole Plasma Concentration
Tidsramme: Day 3
Day 3

Samarbeidspartnere og etterforskere

Det er her du vil finne personer og organisasjoner som er involvert i denne studien.

Sponsor

Samarbeidspartnere

Studierekorddatoer

Disse datoene sporer fremdriften for innsending av studieposter og sammendragsresultater til ClinicalTrials.gov. Studieposter og rapporterte resultater gjennomgås av National Library of Medicine (NLM) for å sikre at de oppfyller spesifikke kvalitetskontrollstandarder før de legges ut på det offentlige nettstedet.

Studer hoveddatoer

Studiestart (Antatt)

30. oktober 2026

Primær fullføring (Antatt)

31. oktober 2028

Studiet fullført (Antatt)

31. oktober 2028

Datoer for studieregistrering

Først innsendt

19. oktober 2026

Først innsendt som oppfylte QC-kriteriene

4. november 2026

Først lagt ut (Faktiske)

10. november 2026

Oppdateringer av studieposter

Sist oppdatering lagt ut (Faktiske)

10. november 2026

Siste oppdatering sendt inn som oppfylte QC-kriteriene

4. november 2026

Sist bekreftet

1. november 2026

Mer informasjon

Begreper knyttet til denne studien

Plan for individuelle deltakerdata (IPD)

Planlegger du å dele individuelle deltakerdata (IPD)?

NEI

Legemiddel- og utstyrsinformasjon, studiedokumenter

Studerer et amerikansk FDA-regulert medikamentprodukt

Ja

Studerer et amerikansk FDA-regulert enhetsprodukt

Nei

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