Bacteriophage Therapy of Difficult-to-treat Infections

Bacterial Infections Clinical Trial

— BT100  

Official title:

Bacteriophage Therapy of Difficult-to-treat Infections: a Retrospective, Observational Analysis of the First One Hundred Consecutive Cases Facilitated by a Belgian Consortium

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT05498363
• Other study ID #: BT100
• Status: Completed
• Start date: January 1, 2008
• Est. completion date: December 31, 2021

Study information

• Verified date: August 2022
• Source: Queen Astrid Military Hospital
• Contact: n/a
• Is FDA regulated: No
• Study type: Observational

Clinical Trial Summary

A retrospective, observational analysis of the first one hundred consecutive cases of bacteriophage therapy of difficult-to-treat infections, facilitated by a Belgian consortium.

Description:

Background: In 2008, the Queen Astrid military hospital (QAMH) re-initiated treatments with phages, in selective cases. The QAMH implemented a Phage Therapy Coordination Center (PTCC), which is an essential step in the re-introduction of safe and efficient phage therapy, in collaboration with several hospitals and the public health authorities.

In 2018, Belgium implemented a pragmatic phage therapy framework that centers on the magistral preparation (compounding pharmacies in the US) of tailor-made phage medicines, which paved the way for a broader and more structured application of phages in Belgium.

The PTCC facilitated phage therapy in about 110 difficult-to-treat infections in patients in Belgium, but also abroad, as the Belgian is increasingly finding appeal in other European countries.

Objective: The goal of this study is to retrospectively analyse observational data on the first one hundred consecutive phage therapy cases of difficult-to-treat infections, which were facilitated by the PTCC. The knowledge gained from these cases would help physicians to select effective treatment protocols and to design new clinical trials.

Study design: A de-identified database consisting of demographical, microbiological and clinical observational data on 100 consecutive phage applications performed between 01/01/2008 and 31/05/22 will be retrospectively analyzed. A list of the parameters that will be analyzed can be found in addendum 1.

According to the EU Regulation No 536/2014 (Clinical Trials Regulation) and its transposition to Belgian Law, the retrospective non-interventional study of the de-identified existing phage therapy database is not considered as a an experiment on the human person and does not require informed consent.

The R software environment will be used to analyze the correlation between treatment variables, including the applied phage products (used in combination with antibiotics or not), clinical protocols (proposed by the PTCC, and mostly based on the experiences of the Eliava Institute in the Republic of Georgia), infection types, possible adverse events, clinical outcome (improvement or not), and microbial eradication.

Results will be translated into practical recommendations, which will help physicians to select effective treatment protocols and to design new clinical trials.

The quality control of the used phage products was performed by Sciensano (formerly known as the Belgian Scientific Institute for Public Health) and clinical applications were performed in 34 hospitals in 12 countries (Belgium, United Kingdom, Germany, France, The Netherlands, Switzerland, Latvia, Tunisia, Spain, Portugal, Italy and Austria), under four different regulatory frameworks:

1. Standard of care with magistral phage preparations (since 2018)

2. Article 37 (unproven interventions in clinical practice) of the Declaration of Helsinki

3. Standard of care with unlicensed medicines (in the United Kingdom)

4. "Autorisation Temporaire d'Utilisation" (ATU) (in France) Written informed consent for the clinical application of phages was obtained from the involved patients or their legal representatives according to local provisions. Where warranted, local ethical committee approval for the application of phage therapy was obtained.

The data was obtained through the patients' treating physicians and their authorisation to analyse this data, and a possible scientific publication of the results of this study, will be obtained.

The study is conducted at the QAMH in Brussels under the responsibility and supervision of Dr. Sarah Djebara of the PTCC of the QAMH.

Addendum 1. Observational data on the 100 consecutive phage therapy cases

Demographics*:

Country in which the therapy was performed/ Year in which phage therapy was initiated/ Patient gender/ Patient age

Infection:

Primary infection type/ Secondary infection type/ Acute or chronic infection?/ Additional relevant information/ Organisms/ Antibiotic resistance profile of the targeted strain(s)

Phage product:

Phage name(s)/ Diluent/ Concentration (pfu/ml)

Treatment:

Intraoperative application/ Application route 1 (Dose/Duration)/ Application route 2 (Dose/Duration)/ Concomitant antibiotic treatment/ Ambulatory or hospitalized?

Adverse events:

Adverse event/Duration/Severity/Relationship to phage treatment?/Action

Clinical outcome:

Clinical improvement?/Microbial eradication?/Clinical comment (additional relevant information)

Regulatory context

Published case? If yes, reference

• The demographics data are separated from the individual cases

Recruitment information / eligibility

• Status: Completed
• Enrollment: 100
• Est. completion date: December 31, 2021
• Est. primary completion date: December 31, 2021
• Accepts healthy volunteers: No
• Gender: All
• Age group: 1 Month to 91 Years

Eligibility

Inclusion Criteria:

• Patients with difficult-to-treat bacterial infections

Exclusion Criteria:

• None

Related Conditions & MeSH terms

• Bacterial Infections
• Communicable Diseases
• Infections

Intervention

Biological:
• Bacteriophage therapy
Difficult-to-treat bacterial infections were treated with bacteriophages (selected from a collection of 25 individual bacteriophages and 6 bacteriophage cocktails), which were shown to target the patient's infecting bacterial strain (in vitro)

Locations

Country	Name	City	State
n/a

Sponsors (1)

Lead Sponsor	Collaborator
Queen Astrid Military Hospital

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Clinical improvement	Clinical improvement of at least one symptom associated with the original bacterial infection, as assessed by the treating physician	One week to one year after treatment, depending on the infection type
Primary	Microbial eradication	The absence of the original causative agent of the bacterial infection in culture	One week to one year after treatment, depending on the infection type
Primary	Adverse reactions	Duration and severity of adverse reactions, as assessed by the treating physician	One week to one year after treatment, depending on the infection type