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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
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.
Studie Overzicht
Toestand
Interventie / Behandeling
Studietype
Inschrijving (Geschat)
Fase
- Fase 3
Contacten en locaties
Studiecontact
- Naam: ISTX Clinical Trials
- Telefoonnummer: 617-715-3600
- E-mail: Clinicaltrials@istx.com
Deelname Criteria
Geschiktheidscriteria
Leeftijden die in aanmerking komen voor studie
Accepteert gezonde vrijwilligers
Geslachten die in aanmerking komen voor studie
Beschrijving
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:
- Based on at least one blood culture obtained within 48 hours prior to randomization that is positive for S. aureus
- 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
Studie plan
Hoe is de studie opgezet?
Ontwerpdetails
- Primair doel: Behandeling
- Toewijzing: Gerandomiseerd
- Interventioneel model: Parallelle opdracht
- Masker: Enkel
Wapens en interventies
Deelnemersgroep / Arm |
Interventie / Behandeling |
|---|---|
|
Experimenteel: 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. |
|
Actieve vergelijker: 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. |
Wat meet het onderzoek?
Primaire uitkomstmaten
Uitkomstmaat |
Tijdsspanne |
|---|---|
|
Percentage of Participants with Treatment-Emergent Adverse Events (TEAEs)
Tijdsspanne: 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)
Tijdsspanne: Baseline through LFU [up to 11 weeks]
|
Baseline through LFU [up to 11 weeks]
|
|
Percentage of participants with treatment-related adverse events (AEs)
Tijdsspanne: 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)
Tijdsspanne: 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
Tijdsspanne: 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
Tijdsspanne: 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
Tijdsspanne: 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
Tijdsspanne: 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
Tijdsspanne: Baseline through LFU visit [up to 11 weeks]
|
Baseline through LFU visit [up to 11 weeks]
|
|
Change from baseline in systolic blood pressure
Tijdsspanne: Baseline through LFU visit [up to 11 weeks]
|
Baseline through LFU visit [up to 11 weeks]
|
|
Change from baseline in diastolic blood pressure
Tijdsspanne: Baseline through LFU visit [up to 11 weeks]
|
Baseline through LFU visit [up to 11 weeks]
|
|
Change from baseline in respiratory rate
Tijdsspanne: Baseline through LFU visit [up to 11 weeks]
|
Baseline through LFU visit [up to 11 weeks]
|
|
Change from baseline in heart rate
Tijdsspanne: Baseline through LFU visit [up to 11 weeks]
|
Baseline through LFU visit [up to 11 weeks]
|
Secundaire uitkomstmaten
Uitkomstmaat |
Maatregel Beschrijving |
Tijdsspanne |
|---|---|---|
|
Percentage of All-Cause Mortality (ACM)
Tijdsspanne: 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
Tijdsspanne: 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
Tijdsspanne: 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
Tijdsspanne: 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
Tijdsspanne: 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
Tijdsspanne: Day 3
|
Day 3
|
Medewerkers en onderzoekers
Sponsor
Medewerkers
Studie record data
Bestudeer belangrijke data
Studie start (Geschat)
Primaire voltooiing (Geschat)
Studie voltooiing (Geschat)
Studieregistratiedata
Eerst ingediend
Eerst ingediend dat voldeed aan de QC-criteria
Eerst geplaatst (Werkelijk)
Updates van studierecords
Laatste update geplaatst (Werkelijk)
Laatste update ingediend die voldeed aan QC-criteria
Laatst geverifieerd
Meer informatie
Termen gerelateerd aan deze studie
Trefwoorden
Aanvullende relevante MeSH-voorwaarden
- Hart-en vaatziekten
- Hartziekten
- Infecties
- Bacteriële infecties
- Bacteriële infecties en mycosen
- Cardiovasculaire infecties
- Endocarditis
- Endocarditis, bacterieel
- Health Services Administration
- Kwaliteit, toegang en evaluatie van de gezondheidszorg
- Kwaliteit van de gezondheidszorg
- Kwaliteitsindicatoren, gezondheidszorg
- Zorgstandaard
- ceftobiprole medocaril
Andere studie-ID-nummers
- CSBAL5788-2025-002
Plan Individuele Deelnemersgegevens (IPD)
Bent u van plan om gegevens van individuele deelnemers (IPD) te delen?
Informatie over medicijnen en apparaten, studiedocumenten
Bestudeert een door de Amerikaanse FDA gereguleerd geneesmiddel
Bestudeert een door de Amerikaanse FDA gereguleerd apparaatproduct
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