Efficacy Of Bacterial Lysate In Asthmatic Children (EOLIA)

Lallemand

Status and phase

Completed

Phase 3

Conditions

Allergic Asthma

Treatments

Biological: ISMIGEN

Biological: PLACEBO

Study type

Interventional

Funder types

Industry

Identifiers

NCT02541331

LPI-1201

Details and patient eligibility

About

This study evaluate the efficacy of Mechanical Bacterial Lysate (PMBL - Ismigen®) to improve the asthma control level (ACT score) as add-on treatment to routine asthma treatment in children aged 6 to 16 with uncontrolled or partly controlled asthma. Half of the 150 participants will receive Ismigen® and their current asthma therapy while the other half will receive Placebo and their current asthma treatment.

Full description

Acute and recurrent respiratory infections of the upper and middle respiratory tracts in the paediatric population of asthmatic patients represent a leading clinical burden, particularly during the winter. Respiratory tract infections, mainly viral infection are important factors that exacerbate asthma course in children. Currently no clinical data demonstrated the benefit of oral or sublingual bacterial lysates on asthma clinical course in children apart from one trial with OM-85 BV (Bronchovaxom®) suggesting reduced number and duration of infection-related wheezing attacks in children with asthma wheezing.

Therefore it was hypothesized that PMBL (Ismigen®) used in asthmatic children should significantly improve asthma course and control. A seasonal approach of active prevention, based on full-fledged antibacterial oral vaccination would be useful to show the potential benefit of this type of products.

The Primary objective was to assess the benefit of Ismigen® versus Placebo on the mean ACT score after administration of a Polyvalent Mechanical Bacterial Lysate (PMBL - Ismigen®) as add-on to routine asthma treatment.

Secondary objectives investigated:

the potential reduction (vs Placebo) of number of asthma exacerbations, time to first event with Ismigen®;
the potential decrease in number of respiratory tract infections during the observation period (3-month treatment and 6-month follow-up) after treatment;
the specific changes occurring in a panel of immunological markers as the result of Ismigen® effect (subset of 48 patients).

Enrollment

150 patients

Sex

All

Ages

6 to 16 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

Children of both genders aged 6 to 16 years.
Allergic asthma diagnosis with at least one perennial allergen according to the Global Strategy for Asthma Management and Prevention (GINA 2012 guidelines) prior to screening visit.
Patient shows clinical characteristics of partly controlled or uncontrolled asthma according to GINA 2012.
Already treated with SABA prn and ICS or ICS + LABA during the previous 3 months.
Patient shows antigen-specific IgE against HDM ≥ class 2 or positive skin prick test or RAST for at least one perennial allergen.
Patient who had at least 2 exacerbations of asthma within the 12-mo period before V1.
Patient not treated with Polyvalent Mechanical Bacterial Lysate (Ismigen®) within the previous 6 months prior to Visit 1.

Exclusion criteria

Patient received mechanical or any other bacterial lysate immunostimulation within the previous 6 months before Visit 1.
Patient received oral/subcutaneous allergen-immunotherapy within the previous 6 months before Visit 1.
History of near fatal asthma (e.g. brittle asthma, hospitalization for asthma exacerbation in Intensive Care Unit).
Pregnant or breastfeeding woman.