Dalbavancin Versus Standard Antibiotic Therapy for Catheter-related Bloodstream Infections Due to Staphylococcus Aureus

NCT ID: NCT05117398

Last Updated: 2025-04-06

Basic Information

• Recruitment Status: RECRUITING
• Clinical Phase: PHASE3
• Total Enrollment: 406 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2023-06-23
• Study Completion Date: 2026-09-23

Brief Summary

The primary objective of the study is to demonstrate, among patients with non-complicated CR-BSIs due to S. aureus, that a single-dose of intravenous (IV) dalbavancin 1500 mg is non-inferior to standard documented antibiotic therapy for 14 days according to national guidelines at DAY 30 (Long follow up visit).

As the secondary objectives, the study aims to evaluate according to treatment group:

1. Cure rate at DAY 14 and DAY 90 (EOS);

2. Mortality rate within 90 days of follow-up;

3. Time to negativation of blood cultures;

4. Patient's quality of life;

5. Hospitalization length of stay;

6. Cost-utility analyses;

7. Occurrence of any adverse event (AE and SAE), until Day 90 (EOS).

Detailed Description

Catheter-related bloodstream infections (CR-BSIs) are the most common nosocomial bloodstream infections, with an incidence as high as 8.5 to 19.8 infections per 1000 catheter-days. Staphylococcus aureus is involved in about 20% of CR-BSIs and associated with significant morbidity, mortality (9.3%), prolonged hospital stay (+ 9 days), and healthcare costs (35 000 € to 65 000 € per case). S. aureus CR-BSIs occurs mainly in frail patients with a port of catheter for chemotherapy or parenteral nutrition.

According to international guidelines, management of CR-BSIs due to S. aureus includes the removal and replacement of the infected catheter and a 14-day intravenous (IV) antibiotic therapy. Therefore, the management of CR-BSIs due to S. aureus requires the insertion of a new intravenous catheter. In turn, the new catheter can also lead to new septic complications and limit the patients' autonomy. Non-adherence to these recommendations leads to over-mortality and costs.

Following of the positive results of the SABATO trial in 2021 to determine whether early switch to oral antibiotic therapy is safe and effective in patients with uncomplicated BSA, oral switch during staphylococcal bacteremia, will likely become the standard of care. It is therefore justified to allow oral switch in the control arm.

The usual practice in some centers is already to switch to oral antibiotics, after a minimum of 7 days of intravenous treatment.

Dalbavancin is a new glycopeptide antibiotic, with an excellent bactericidal activity against Gram-positive bacteria, especially S. aureus, and a prolonged half-life of 14 to 15 days. As a comparison, half-life of antibiotics usually used for CR-BSIs due to S. aureus, i.e. penicillin or glycopeptide, as-per sensitivity to methicillin is much lower: 1.5 to 9 hours. Such prolonged half-life allows one IV injection to be sufficient and effective over 14 days of treatment. This remarkable characteristic should allow patients to be promptly discharged from hospital without monitoring.

The hypothesis of the study is that in patients with CR-BSIs due to S. aureus, after catheter removal, dalbavancin could be administered intravenously in a single administration after catheter removal and be as effective as standard documented antibiotic therapy for 14 days according to national guidelines.

Conditions

Catheter Bacteremia; Staphylococcus Aureus Infection

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Study Groups

Dalbavancin

Dalbavancin (Xydalba®) 1500 mg - One unique dose

Group Type: EXPERIMENTAL

Dalbavancin administration

Intervention Type: DRUG

A single-dose of intraveneuse (IV) administration of dalbavancin of 1500 mg.

In case of patients with chronic renal impairment (creatinin clairance < 30mL/min), a single-dose of IV administration of reduced dalbavancin of 1000 mg.

Standard documented antibiotic therapy for 14 days according to national guidelines.

As currently recommended, investigators will be encouraged to use the intravenous route for the entire duration of treatment. However, in order to interfere as little as possible with usual practice in each center, the antimicrobial therapy will be let to the choice of the physician in charge of the patient after a minimum of 7 days of intravenous treatment.

During all the duration of the study, in case of worsening of the clinical condition requiring the prescription of antistaphylococcal, the clinician will prescribe additional antibiotherapy according to standard good practice.

Group Type: ACTIVE_COMPARATOR

Standard antibiotic therapy

Intervention Type: DRUG

Standard Antibiotic therapy according to national recommendations. During the study, the start of treatment is considered to be the day of inclusion/randomization (even if active antiobiotic treatment was started, less than 72 hours ago according to inclusion criteria).

Interventions

Dalbavancin administration

A single-dose of intraveneuse (IV) administration of dalbavancin of 1500 mg.

In case of patients with chronic renal impairment (creatinin clairance < 30mL/min), a single-dose of IV administration of reduced dalbavancin of 1000 mg.

Intervention Type: DRUG

Standard antibiotic therapy

Standard Antibiotic therapy according to national recommendations. During the study, the start of treatment is considered to be the day of inclusion/randomization (even if active antiobiotic treatment was started, less than 72 hours ago according to inclusion criteria).

Intervention Type: DRUG

Other Intervention Names

Xydalba® administration; Standard documented antibiotic therapy

Eligibility Criteria

Inclusion Criteria

• Patients aged at least 18 years;
• Blood cultures positive for S. aureus, obtained within 72 hours before randomization (the date considered is the date of the sampling, not the results);
• CR-BSI, defined as:

• One positive blood culture AND Local signs of infection at the catheter site; OR
• at least one positive blood culture obtained from the catheter and the peripheral vein; AND
• A differential period between catheter versus peripheral blood culture positivity of at least 2h as recommended; AND
• Same S. aureus isolate (same phenotype) identified from the catheter and the peripheral vein blood cultures; OR
• One positive blood culture; AND
• Strong presumption of catheter-related infection according to clinical opinion.
• Intravascular catheter - implantable venous access device (port-a-cath and Piccline) - removed before randomization;
• Informed consent form date and signed by the patient.

Exclusion Criteria

• Polymicrobial infection;
• Dalbavancin resistant strain;
• More than 72 hours of active antibiotic treatment targeting S. aureus (in-vitro susceptibility) administered prior to randomization;
• Patient with known valvulopathy, previous history of endocarditis, or suspicion of infective endocarditis by physician in charge;
• Suspicion of any other deep focus infections, such as arthritis, pneumonia, osteomyelitis, or meningitis, presence of cerebral or peripheral emboli (arterial occlusion);
• Thrombophlebitis;
• Failure to remove any intravascular catheter which was present when first positive blood culture;
• Signs of infection associated with quick SOFA score ≥ 2 at randomization;
• Patients with foreign bodies such as: prosthetic heart valve, endovascular prosthesis, ventriculo-atrial shunt, pacemaker, or an automated implantable cardioverter defibrillator (AICD) device;
• Severe liver disease (Child-Pugh C);
• Severely immunocompromised patients:

• Neutropenia (< 500 neutrophils/µL) at randomization;
• Hematopoietic stem cell transplantation within the past 6 months or planned during treatment period;
• Solid organ transplant;
• Contraindication to dalbavancin and/or glycopeptide;
• Life expectancy < 3 months;
• Active injection drug user;
• Pregnant or breastfeeding women;
• For premenopausal women: failure to use highly-effective contraceptive methods for 1 month after receiving study drug;
• Participation in other interventional trials ongoing;
• Persons held in an institution by legal or official order;
• Patients under legal protection;
• Patients under guardianship or curators;
• Patients unable to give a free and informed consent;
• Patient not affiliated to a social security scheme: obligation of affiliation to a social security scheme or to be a beneficiary.

• Minimum Eligible Age: 18 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Centre Hospitalier de Perigueux

OTHER

Sponsor Role: collaborator

Advanz Pharma

INDUSTRY

Sponsor Role: collaborator

Nantes University Hospital

OTHER

Sponsor Role: collaborator

Centre National de Référence des staphylocoques

UNKNOWN

Sponsor Role: collaborator

Assistance Publique - Hôpitaux de Paris

OTHER

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Bernard CASTAN, MD

Role: PRINCIPAL_INVESTIGATOR

CH de Perigueux

Aurélien DINH, MD, PhD

Role: STUDY_DIRECTOR

APHP - RAYMOND POINCARE

Locations

Infectious Diseases Department, Raymond-Poincaré Hospital - APHP

Garches, , France

Site Status: NOT_YET_RECRUITING

Infectious Diseases Department, CH PERIGUEUX

Périgueux, , France

Site Status: RECRUITING

Countries

France

Central Contacts

Bernard CASTAN, MD

Role: CONTACT

bernard.castan@ch-perigueux.fr

+33 5 53 45 26 00

Aurélien DINH, MD, PhD

Role: CONTACT

aurelien.dinh@aphp.fr

+33 1 47 10 44 32

Facility Contacts

Aurelien DIHN, MD, PhD

Role: primary

Bernard CASTAN, MD

Role: primary

Other Identifiers

2021-004038-12

Identifier Type: EUDRACT_NUMBER

Identifier Source: secondary_id

APHP220763

Identifier Type: -

Identifier Source: org_study_id