Evidence map›Paper›PMID 32504314›Full record

ArticleEuropean journal of clinical microbiology & infectious diseases : official publication of the European Society of Clinical Microbiology2020

Analysis of C. difficile infection-related outcomes in European participants in the bezlotoxumab MODIFY I and II trials.

Emilio Bouza, Oliver A Cornely, Antonio Ramos-Martinez, Robert Plesniak, Misoo C Ellison, Mary E Hanson, Mary Beth Dorr

2 registry-linked trialsOpen access · hybridAbstract read
In one paragraph

Article in European journal of clinical microbiology & infectious diseases : official publication of the European Society of Clinical Microbiology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 2 registered trials, which are not on this map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.2field-weighted citation impact, top 37% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

NCT01241552 phase3completednot on this map

A Phase III, Randomized, Double-Blind, Placebo-Controlled, Adaptive Design Study of the Efficacy, Safety, and Tolerability of a Single Infusion of MK-3415 (Human Monoclonal Antibody to Clostridium Difficile Toxin A), MK-6072 (Human Monoclonal Antibody to Clostridium Difficile Toxin B), and MK-3415A (Human Monoclonal Antibodies to Clostridium Difficile Toxin A and Toxin B) in Patients Receiving Antibiotic Therapy for Clostridium Difficile Infection (MODIFY I)

TypeinterventionalSponsorMerck Sharp & Dohme LLCRan2011 to 2014Enrolled1,452ConditionsClostridium Difficile InfectionArmsMK-3415, MK-6072, MK-3415A, Placebo, SOC
NCT01513239 phase3completednot on this map

A Phase III, Randomized, Double-Blind, Placebo-Controlled Study of the Efficacy, Safety and Tolerability of a Single Infusion of MK-6072 (Human Monoclonal Antibody to Clostridium Difficile Toxin B), and MK-3415A (Human Monoclonal Antibodies to Clostridium Difficile Toxin A and B) in Patients Receiving Antibiotic Therapy for Clostridium Difficile Infection (MODIFY II)

TypeinterventionalSponsorMerck Sharp & Dohme LLCRan2012 to 2015Enrolled1,203ConditionsClostridium Difficile InfectionArmsMK-6072, MK-3415A, Placebo, SOC
3 · Its place in the literature

Who cites it

2 citing papers in PubMed, 8 citations in OpenAlex.

  1. Genomic epidemiology and transmission dynamics of recurrent Clostridioides difficile infection in Western Australia.European journal of clinical microbiology & infectious diseases : official publication of the European Society of Clinical Microbiology · 2023
    Article
  2. The Role of Bezlotoxumab for the Prevention of RecurrentAntibiotics (Basel, Switzerland) · 2022
    Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors at 5 institutions in 4 countries.

Emilio BouzaUniversity Complutense of Madrid, Madrid, Spain.
Oliver A CornelyFaculty of Medicine and University Hospital Cologne, Department I of Internal Medicine, Excellence Center for Medical Mycology (ECMM); Cologne Excellence Cluster on Cellular Stress Responses in Aging-Associated Diseases (CECAD); Clinical Trials Centre Cologne (ZKS Köln), University of Cologne, Cologne, Germany.
Antonio Ramos-MartinezHospital Universitario Puerta de Hierro-Majadahonda, Madrid, Spain.
Robert PlesniakUniversity of Rzeszów Medical Center, Łańcut, Poland.
Misoo C EllisonMerck & Co., Inc., 2000 Galloping Hill Road, Kenilworth, NJ, 07033, USA.
Mary E HansonMerck & Co., Inc., 2000 Galloping Hill Road, Kenilworth, NJ, 07033, USA.
Mary Beth DorrMerck & Co., Inc., 2000 Galloping Hill Road, Kenilworth, NJ, 07033, USA. mary.beth.dorr@merck.com.
Merck & Co., Inc., Rahway, NJ, USA (United States) · USHospital Universitario Puerta de Hierro Majadahonda · ESRzeszów University · PLUniversidad Complutense de Madrid · ESUniversity Hospital Cologne · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The MODIFY I/II trials demonstrated that bezlotoxumab, a human monoclonal antibody against Clostridioides difficile toxin B, given during antibiotic treatment for Clostridioides difficile infection (CDI) significantly reduced C. difficile recurrence (rCDI) in adults at high risk for rCDI. Efficacy of CDI-directed intervention may depend on ribotype regional epidemiology, and patient characteristics. This post hoc analysis assessed the efficacy of bezlotoxumab in the subgroup of MODIFY I/II trial participants enrolled in Europe. Data from the bezlotoxumab (10 mg/kg single intravenous infusion) and placebo (0.9% saline) groups from MODIFY I/II were compared to assess initial clinical cure (ICC), rCDI, all-cause, and CDI-associated rehospitalizations within 30 days of discharge, and mortality through 12 weeks post-infusion. Of 1554 worldwide participants, 606 were from Europe (bezlotoxumab n = 313, 51%; placebo n = 292; 48%). Baseline characteristics were generally similar across groups, although there were more immunocompromised participants in the bezlotoxumab group (27.2%) compared with placebo (20.1%). Fifty-five percent of participants were female, and 86% were hospitalized at randomization. The rate of ICC was similar between treatment groups. The rate of rCDI in the bezlotoxumab group was lower compared with placebo among European participants overall, and among those with ≥ 1 risk factor for rCDI. Bezlotoxumab reduced 30-day CDI-associated rehospitalizations compared with placebo. These results are consistent with overall results from the MODIFY trials and demonstrate that bezlotoxumab reduces rCDI and CDI-associated rehospitalizations in European patients with CDI. MODIFY I/II (NCT01241552 and NCT01513239).

Indexed as

AdolescentAdultAgedAged, 80 and overAnti-Bacterial AgentsAntibodies, MonoclonalBacterial ProteinsBacterial ToxinsBroadly Neutralizing AntibodiesClostridium InfectionsCross InfectionDrug CombinationsEuropeFemaleHumansInfusions, IntravenousAnti-Bacterial AgentsAntibodies, MonoclonalBacterial ProteinsBacterial ToxinsbezlotoxumabBroadly Neutralizing AntibodiesDrug CombinationstoxB protein, Clostridium difficileBezlotoxumabCDI recurrenceClostridioides difficile infectionRehospitalization

Identifiers

PMID32504314
PMCPMC7497347
OpenAlexW3033048555

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.