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Real-world Evaluation of Bezlotoxumab for the Management of Clostridioides Difficile Infection

Real-world Evaluation of Bezlotoxumab for the Management of Clostridioides Difficile Infection

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04317963
Enrollment
180
Registered
2020-03-23
Start date
2020-02-12
Completion date
2023-02-22
Last updated
2023-02-28

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

Conditions

Clostridium Difficile Infection, Clostridium Difficile Infection Recurrence

Brief summary

This is a retrospective case:control study examining the use of adjunctive bezlotoxumab to standard C. difficile infection (CDI) treatment compared to standard CDI treatment alone in patients with CDI seen in an academic medical center's specialty outpatient clinic.

Detailed description

This specialty clinic is a unique practice setting where patients with ≥1 recurrent CDI and/or refractory disease are referred. The study will represent real-world data on the clinical use of bezlotoxumab as adjunctive therapy in combination with vancomycin or fidaxomicin for the treatment of patients with recurrent CDI. Retrospective chart review will be conducted for patients who visited the specialty CDI clinic between 1/1/2005 through 12/5/2019. Case patients will be defined as patients who have received bezlotoxumab 10 mg/kg intravenously in addition to standard CDI treatment. Controls will be defined as patients who have received only standard CDI treatment and will be enrolled in a 2:1 ratio to cases. The primary outcome is recurrence of CDI. Recurrence is defined as a new episode of C. difficile infection that occurs after the initial clinical cure of the baseline episode within 12 weeks of receipt of bezlotoxumab or standard CDI treatment. Clinical cure is defined as no diarrhea for 2 consecutive days after completion of standard-of-care CDI therapy. Recurrent CDI will be diagnosed via clinical signs and symptoms and CDI diagnostic assay.

Interventions

BIOLOGICALBezlotoxumab

Bezlotoxumab 10 mg/kg IV infusion in addition to standard CDI treatment

DRUGStandard CDI treatment

Standard CDI treatment includes one or a combination of oral vancomycin, oral vancomycin taper and/or pulse, fidaxomicin, and fidaxomicin taper and/or pulse

Sponsors

Merck Sharp & Dohme LLC
CollaboratorINDUSTRY
University of Illinois at Chicago
Lead SponsorOTHER

Study design

Observational model
CASE_CONTROL
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

(Cases): * Age 18 years and older * Diagnosis of C. difficile infection by clinical signs and symptoms and/or C. difficile diagnostic assay * Received bezlotoxumab in addition to standard CDI treatment Inclusion Criteria (Controls): * Age 18 years and older * Diagnosis of C. difficile infection by clinical signs and symptoms and/or C. difficile diagnostic assay * Received only standard CDI treatment

Exclusion criteria

* Diarrhea due to causes other than C. difficile * Incomplete documentation in the electronic medical record

Design outcomes

Primary

MeasureTime frameDescription
Rate of CDI Recurrencewithin 12 weeks of receipt of bezlotoxumabNew episode of C. difficile infection that occurs after initial clinical cure of the baseline episode within 12 weeks of receipt of bezlotoxumab or completion of standard CDI treatment.

Secondary

MeasureTime frameDescription
Clinical cure2 consecutive days after completion of standard-of-care CDI therapy.Clinical cure is defined as no diarrhea for 2 consecutive days after completion of standard-of-care CDI therapy.

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026