Prevention With Ismigen of RTIs in Kids

Respiratory tract infections (RTIs) are the leading cause of acute disease incidence worldwide that affect people of all ages. They are usually caused by viral pathogens, the most common of which including rhinoviruses, coronaviruses, adenoviruses, respiratory syncytial virus and influenza viruses. Bacterial pathogens can also cause RTIs, but they are less common. Various studies show the seasonality of RTIs. Influenza tends to occur in late autumn and winter, while other RTIs have a much more diffuse occurrence throughout the year. Although RTIs are usually not life-threatening, they significantly decrease quality of life and represent a substantial proportion of healthcare visits, mainly in women and young children, contributing to a financial burden on society.

Ismigen® (Polyvalent Mechanical Bacterial Lysate; PMBL) which is manufactured by mechanical lysis is currently authorized in two EU Member States (MS), Italy and Poland, where Lallemand Pharma Europe is the Marketing Authorization Holder (MAH) as sublingual tablets for the prophylaxis of recurrent RTI in adults. It is authorized in Poland in children from 3 years of age.

On 27 June 2019, the European Medicines Agency (EMA) recommended that bacterial lysates-containing medicinal products authorized for respiratory conditions should only be used for the prevention of recurrent respiratory tract infections, with the exception of pneumonia. This followed a review in which EMA's human medicines committee (CHMP) considered the results of clinical studies, data on side effects reported with these medicines, and advice from an expert group on infectious diseases. Although data are limited, the review found some evidence of effectiveness of bacterial lysates in the prevention of recurrent RTI together with a safety profile in line with what is expected for this type of product. The CHMP therefore recommended that use of bacterial lysates for prevention can continue, but the companies must provide further data on safety and effectiveness by Q1 2026 through the conduct of phase IV double-blind, multicenter, RCTs in this indication.

The present study is a Post-Authorization Efficacy Study (PAES) designed to demonstrate that PMBL® sublingual tablet used according to the SmPC instructions can reduce the incidence of respiratory tract infections in children 3 to 12 years old during the fall and winter period when compared to a matched Placebo.

Inclusion criteria

• Children of both genders aged from 3 to 12 years.
• Written informed consent obtained from the parents/legally authorized representatives
• Written assent obtained from the subject from 7 years
• Subject presenting with a susceptibility to respiratory tract infections according to the investigator
• No respiratory tract infection within 15 days before the randomization visit
• All girls of childbearing potential have a negative pregnancy urine testing at randomization visit and are informed and their parents as well of the requirement for contraception during the study.
• A cooperative attitude and ability to correct use of PMBL® tablet.

Exclusion criteria

• Subject treated with bacterial lysates within the previous 6 months prior to V1 or ongoing treatment.
• Body temperature ≥ 37.5°C at the randomization visit.
• Pregnant/Lactating female or with sexual activity without hormonal contraception, intrauterine device or barrier methods.
• Primary or secondary immunodeficiency, cystic fibrosis, bronchiectasis, alpha-1 antitrypsin deficiency, malignancy, endocrinological diseases or other chronic respiratory diseases, except asthma and allergic rhinitis.
• Known sensitivity to the components of study medication.
• Any major surgery within the last 3 months prior to study enrolment or planned to occur within the duration of study.
• Treatment with the following medications:

• Injection or oral administration of steroids within 4 weeks prior to study enrolment.
• Previous and/or concomitant immunosuppressants, immunostimulants, allergen-immunotherapy or gamma globulins within 6 months prior to study enrolment.
• Inability to understand or comply with study procedures or with study treatment intake.
• Subject participating in another interventional clinical study at the time of screening visit.