Clinical trial

Bezlotoxumab Yielded Outcomes by Addressing Personalized Needs in Clostridioides Difficile Infection: The BEYOND Double-Blind Randomized Clinical Trial

Name
BEYOND
Description
Previous data have shown that integrated information from single nucleotide polymorphisms (SNPs) of the host DNA, interleukin 8 (IL-8) and the enrichment of the stool microbiome can indicate the patients with infection by Clostridioides difficile (CDI) who are at risk for unfavorable outcome. This integrated information is forming the BEYOND score. The aim of the BEYOND randomized clinical trial (RCT) is to investigate if adjunctive bezlotoxumab treatment to the current standard-of-care may decrease the likelihood of unfavorable outcome for patients who score positive by the BEYOND score.
Trial arms
Trial start
2022-04-13
Estimated PCD
2023-06-04
Trial end
2023-06-04
Status
Completed
Phase
Early phase I
Treatment
Bezlotoxumab
Single intravenous infusion of bezlotoxumab
Arms:
Bezlotoxumab
Other names:
Standard-of-care treatment according to local guidelines or to the decision of the attending physicians.
Normal saline 0.9% or 5% dextrose water
Single intravenous infusion - Placebo arm
Arms:
Placebo
Other names:
Standard-of-care treatment according to local guidelines or to the decision of the attending physicians
Size
44
Primary endpoint
Comparison of bezlotoxumab over placebo on reducing the incidence of progression into organ dysfunction defined as any increase of the baseline total SOFA score by at least 2 points.
40 days
Comparison of bezlotoxumab over placebo on reducing the incidence of relapse of Clostridioides difficile infection
40 days
Comparison of bezlotoxumab over placebo on reducing the incidence of death
40 days
Eligibility criteria
Inclusion Criteria: 1. Age equal to or above18 years. 2. Both genders. 3. Written informed consent provided by the patient or by their legal representative in case of patients unable to consent. 4. In case of non-menopausal women, unwillingness to become pregnant during the study period. Women of child-bearing potential will be screened by a urine pregnancy test before inclusion in the study. 5. Diarrhea defined as at least 3 episodes of unformed stool in the past 24hours. 6. Positive stool for C.difficile. This is defined as any stool sample positive for the presence of glutamate dehydrogenase (GDH) and for the presence of toxin A and/or B. 7. Positive BEYOND score i.e. meeting any of the following: Gene score for susceptibility to CDI more than 53. The score is provided by the following equation: (Carriage of C allele of rs12148744 x 27) - (carriage of C allele of rs714024 x 27) - (carriage of C allele of rs721059 x 29) + (carriage of T allele of rs4311028 x 33) - (carriage of A allele of rs62183547 x 25) + (carriage of C allele of rs1128266 x 12) - (carriage of T allele of rs4279595 x 17) + (carriage of G allele of rs175006 x 11) + (carriage of T allele of rs3859214 x 17) + (carriage of G allele of rs7222870 x 15) - (carriage of G allele of rs5086600 x 9) + (carriage of T allele of rs7240534 x 12) + (carriage of G allele of rs20911172 x 11) - (carriage of C allele of rs17680671 x 17) OR Score provided by the following equation more than 9: \[Hemoglobin \<9.5 g/dl x 10\] + \[serum urea \>64.5 mg/dl x 14\] + \[serum interleukin-8 \>227 pg/ml x 19\] - \[carriage of G allele of rs2091172 x 17\] OR More than 3log10 of gammaproteobacteria or Enterobacteriaceae or Enterobacteriales in the stool Exclusion Criteria: * Age below 18 years * Denial for written informed consent * Known allergy to bezlotoxumab * Pregnancy or lactation. Women of child-bearing potential will be screened by a urine pregnancy test before inclusion in the study
Protocol
{'studyType': 'INTERVENTIONAL', 'phases': ['PHASE2'], 'designInfo': {'allocation': 'RANDOMIZED', 'interventionModel': 'PARALLEL', 'interventionModelDescription': 'This is a prospective, 1:1 randomized, double-blind, placebo-controlled trial', 'primaryPurpose': 'TREATMENT', 'maskingInfo': {'masking': 'QUADRUPLE', 'whoMasked': ['PARTICIPANT', 'CARE_PROVIDER', 'INVESTIGATOR', 'OUTCOMES_ASSESSOR']}}, 'enrollmentInfo': {'count': 44, 'type': 'ACTUAL'}}
Updated at
2023-12-15

1 organization

2 products

5 indications

Indication
Mortality