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Clinical Trials/NCT01420744
NCT01420744
Completed
Phase 2

A Randomized, Double-blind, Placebo-controlled, Multicenter, Parallel-group, Adaptive Group-sequential Phase II Study, to Determine the Efficacy and Safety of BT086 as an Adjunctive Treatment in Severe Community Acquired Pneumonia (sCAP)

Biotest36 sites in 4 countries160 target enrollmentAugust 2011

Overview

Phase
Phase 2
Intervention
BT086
Conditions
Community Acquired Pneumonia
Sponsor
Biotest
Enrollment
160
Locations
36
Primary Endpoint
Ventilator Free Days (VFDs)
Status
Completed
Last Updated
10 years ago

Overview

Brief Summary

The purpose of this study is to determine whether the adjunctive therapy to standard antibiotic treatment of BT086 is safe and effective of decreasing the days patients require endotracheal ventilation due to Severe Community-Acquired Pneumonia (sCAP).

Detailed Description

Severe Community-Acquired Pneumonia (sCAP) is usually defined clinically as pneumonia acquired from outside the hospital (CAP) that requires intensive medical care. Mortality of (s)CAP patients admitted to ICU range from 35-58% depending on time and admission of the patient and has not much improved in the last years. BT086 contains a sufficient number of antibodies against the most frequent pathogens as well as antibodies against lipopolysaccharides and lipid A. Therefore, it can be assumed that administration of BT086 early in the clinical course of a severe infection such as sCAP may provide an effective adjunctive treatment to standard antibiotic therapy for sCAP patients.

Registry
clinicaltrials.gov
Start Date
August 2011
End Date
April 2015
Last Updated
10 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
Biotest
Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Written informed consent:
  • given by the patient or
  • a legal/authorised representative of the patient or
  • a waiver for written informed consent due to emergency situation, in compliance with all local legal requirements.
  • Male or female patients aged 18 years or older
  • Patient receiving adequate antibiotic treatment for pneumonia
  • Prior to endotracheal ventilation and therapy, the patient must have at least one of the following two signs of inflammation:
  • Fever/Hypothermia Fever defined as an oral, tympanic, oesophageal or vesical temperature of \>38°C, tympanic temperature of \>38°C or rectal temperature of \>38.5°C, or hypothermia (rectal temperature \<35.5°C) (measurement with temperature probe or device) or
  • White blood cell (WBC) count \>10,000/mm³ or WBC \<4,500/mm³
  • Patient must have at least one of the following signs and symptoms of pneumonia:

Exclusion Criteria

  • For incapacitated patients: any indication that the patient's presumed will would be against inclusion in the trial
  • Patients with suspected hospital-acquired pneumonia
  • Severe lung diseases interfering with sCAP therapy e.g. patients with cystic fibrosis,
  • Patients receiving Xigris® (drotrecogin alfa, activated Protein C) or medications not approved for sCAP (e.g. Dornase alpha) are excluded from inclusion in the study
  • Patients on dialysis
  • Presence of other severe diseases impairing life expectancy (e.g. patients are not expected to survive 28 days given their pre-existing uncorrectable medical condition).
  • Patients unable to be treated due to obesity
  • Selective, absolute IgA deficiency with known antibodies to IgA
  • Patients with neutrophil count \<1,000/mm³ or platelet count \<50,000/mm³
  • Pregnant or lactating women. A pregnancy test will be performed in all women aged \<65 years and the result must be available at study inclusion.

Arms & Interventions

BT086 infusion

Intervention: BT086

1% Human Albumin infusion

Intervention: 1% Human Albumin infusion

Outcomes

Primary Outcomes

Ventilator Free Days (VFDs)

Time Frame: 28 days

VFDs are defined as the number of days between successful weaning from endotracheal ventilation and day 28 after study enrolment.

Secondary Outcomes

  • 28-day pneumonia-cause mortality(28 days (672 hours from randomization))
  • Time (days) to discharge from ICU(28 days)
  • Time (days) to discharge from hospital(28 days)
  • SOFA: Score Sequential Organ Failure Assessment(28 days)
  • Vasopressor-free days(28 days)
  • Glasgow Coma Score(28 days)
  • 28-day all cause mortality(28 days (672 hours from randomization))

Study Sites (36)

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