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Prevention of OM-85 on Bronchiectasis Exacerbation

To Investigate the PRevention of OM-85 on Bronchiectasis Exacerbation (iPROBE): a Multicenter, Randomised, Double-dummy, Placebo-controlled Clinical Trial in Chinese Patients

Status
Completed
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01968421
Enrollment
196
Registered
2013-10-24
Start date
2015-03-01
Completion date
2018-11-23
Last updated
2020-04-21

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Bronchiectasis With Acute Exacerbation

Keywords

OM-85, bronchiectasis, placebo, acute exacerbation

Brief summary

Non-cystic fibrosis bronchiectasis is characterized by irreversible dilatation of the medium-sized bronchi as a result of airway injury due to recurrent or chronic inflammation and infection. Bronchiectasis airways are often colonized with bacterial species. Infections of the airways are thought to play an important role in bronchiectasis exacerbation. The non-specific prevention of recurrent airway infections by immunostimulating agents has gained growing scientific interest. OM-85, consisting extracts of eight kinds of bacteria important in respiratory infections, has shown the benefit for significantly reducing the incidence of exacerbations of chronic obstructive pulmonary disease (COPD). The purpose of this study is to investigate the PReventive effect of OM-85 on Bronchiectasis Exacerbation in Chinese patients (iPROBE). This study is designed as a prospective randomised double-blind placebo-controlled multi-centred trial.

Detailed description

Bronchiectasis is still a common chronic respiratory disease. Non-cystic fibrosis bronchiectasis is characterized by irreversible dilatation of the medium-sized bronchi as a result of airway injury due to recurrent or chronic inflammation and infection. Clinical features of bronchiectasis include chronic production of sputum often mucopurulent or purulent in nature, persistent bacterial colonization, recurrent lower respiratory tract infections. Bronchiectasis airways are often colonized with bacterial species. Infections of the airways are thought to play an important role in bronchiectasis exacerbation. Progressive lung damage in bronchiectasis results from a 'vicious cycle' of recurrent bacterial infection and a deregulated inflammatory response. The non-specific prevention of recurrent airway infections by immunostimulating agents has gained growing scientific interest. OM-85, consisting extracts of eight kinds of bacteria important in respiratory infections, has been known to support the respiratory tract resistance to the pathogens via activating pulmonary macrophages, increasing the ratio of CD4 to CD8 lymphocytes, and changing the level of a variety of cytokines in the lung. OM-85 has shown the benefit for significantly reducing the incidence of exacerbations of chronic obstructive pulmonary disease (COPD). Bronchiectasis exacerbations contribute substantially to rapid decline in lung function, reduced quality of life, and the medical costs. The purpose of this study is to investigate the PReventive effect of OM-85 on Bronchiectasis Exacerbation in Chinese patients (iPROBE). This study is designed as a prospective randomised double-blind placebo-controlled multi-centred trial. A total of 244 patients with bronchiectasis, who have had at least one exacerbation of bronchiectasis in the previous year, will be included. The subjects will be randomly received two courses of 7mg of OM-85 or matching placebo to take one oral capsule per day for 10 days a month for 3 consecutive months at the beginning of the study, then 3 months later with the same schedule for 1 year. We will investigate whether long-term therapy with an oral immunostimulant OM-85 can decrease exacerbations in patients with bronchiectasis over 1-year period. Besides, we will assess other outcomes including: the rate of event-based exacerbation, lung function parameters, the total scores on the St George's respiratory questionnaire and coughing, and inflammatory index. We hope that this study will provide novel information on the preventive effects of OM-85 treatment on bronchiectasis exacerbation and will address a knowledge gap for this poorly understood and under-studied disease.

Interventions

DRUGOM-85 BV

two courses of 7mg of OM-85 or matching placebo to take one oral capsule per day for 10 days a month for 3 consecutive months at the beginning of the study, then 3 months later with the same schedule for 1 year.

Sponsors

Peking University
CollaboratorOTHER
Capital Medical University
CollaboratorOTHER
Tianjin Medical University
CollaboratorOTHER
Zhejiang University
CollaboratorOTHER
China Medical University, China
CollaboratorOTHER
Tongji University
CollaboratorOTHER
Wenzhou Medical University
CollaboratorOTHER
Chinese Academy of Medical Sciences
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
QUADRUPLE (Subject, Caregiver, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to 75 Years
Healthy volunteers
No

Inclusion criteria

* An Institutional Review Board (IRB)/Independent Ethics Committee (IEC) approved written Informed Consent form is signed and dated by the subject. The Informed Consent form will be signed. * Subject/legal representative is considered reliable and capable of adhering to the protocol (eg, able to understand and complete diaries), visit schedule or medication intake according to the judgment of the investigator. * Subject with both genders is adult patients (\>18 years) diagnosed with bronchiectasis by high-resolution computed tomography (HRCT) of chest within 3 years of study inclusion having had at least 1 acute exacerbation in the previous year when recruiting.

Exclusion criteria

* History of cystic fibrosis; * Hypogammaglobulinaemia; * Allergic bronchopulmonary aspergillosis; * Active tuberculosis; * Subject has been assigned to treatment in a study of the medication under investigation in this study in the previous 6 months. * Subject has a history of chronic alcohol or drug abuse within the last 6 months. * Subject has any medical or psychiatric condition that, in the opinion of the investigator, could jeopardize or would compromise the subject's ability to participate in this study. * Subject has a known hypersensitivity to any components of OM85. * Recent immunostimulant in last 3 months, cancer, stroke, severe cardiovascular disease, hepatic/kidney impairment, active TB, immuno-related diseases (RA and inflammatory bowel diseases), active ABPA. * Subjects are free to withdraw from the study at any time, without prejudice to their continued care. * Subject develops an illness that would interfere with his/her continued participation. * Subject is noncompliant with the study procedures or medications in the opinion of the investigator. * Subject takes prohibited concomitant medications as defined in this protocol (flu vaccine and pneumococcal vaccine). * Subject withdraws his/her consent. * There will have a confirmation of a pregnancy during the study, as evidenced by a positive pregnancy test. * The sponsor or a regulatory agency requests withdrawal of the subject.

Design outcomes

Primary

MeasureTime frameDescription
Bronchiectasis Exacerbation1 yearthe proportion of acute exacerbations

Secondary

MeasureTime frameDescription
Life Quality1 year(1)St George' s Respiratory Questionnaire (SGRQ); (2)Leicester Cough Questionnaire (LCQ)
Lung Function1 yearLung function parameters: FEV1, FVC, FEV1/FVC;

Other

MeasureTime frameDescription
Rescue Medication1 yearUse of antibiotics and rapid-acting bronchodilator

Countries

China

Participant flow

Recruitment details

March 1, 2015 was the starting date

Participants by arm

ArmCount
OM-85
The subjects will be randomly received two courses of 7mg of OM-85 to take one oral capsule per day for 10 days a month for 3 consecutive months at the beginning of the study, then 3 months later with the same schedule for 1 year. OM-85: two courses of 7mg of OM-85 or matching placebo to take one oral capsule per day for 10 days a month for 3 consecutive months at the beginning of the study, then 3 months later with the same schedule for 1 year.
99
Placebo
The subjects will be randomly received two courses of 7mg of matching placebo to take one oral capsule per day for 10 days a month for 3 consecutive months at the beginning of the study, then 3 months later with the same schedule for 1 year. OM-85: two courses of 7mg of OM-85 or matching placebo to take one oral capsule per day for 10 days a month for 3 consecutive months at the beginning of the study, then 3 months later with the same schedule for 1 year.
97
Total196

Baseline characteristics

CharacteristicOM-85PlaceboTotal
Age, Categorical
<=18 years
0 Participants0 Participants0 Participants
Age, Categorical
>=65 years
24 Participants27 Participants51 Participants
Age, Categorical
Between 18 and 65 years
75 Participants70 Participants145 Participants
Ethnicity (NIH/OMB)
Hispanic or Latino
0 Participants0 Participants0 Participants
Ethnicity (NIH/OMB)
Not Hispanic or Latino
99 Participants97 Participants196 Participants
Ethnicity (NIH/OMB)
Unknown or Not Reported
0 Participants0 Participants0 Participants
Race/Ethnicity, Customized
Race/Ethnicity
99 Participants97 Participants196 Participants
Region of Enrollment
China
99 participants97 participants196 participants
Sex: Female, Male
Female
53 Participants57 Participants110 Participants
Sex: Female, Male
Male
46 Participants40 Participants86 Participants

Adverse events

Event typeEG000
affected / at risk
EG001
affected / at risk
deaths
Total, all-cause mortality
0 / 990 / 97
other
Total, other adverse events
4 / 997 / 97
serious
Total, serious adverse events
2 / 991 / 97

Outcome results

Primary

Bronchiectasis Exacerbation

the proportion of acute exacerbations

Time frame: 1 year

ArmMeasureValue (MEAN)Dispersion
OM-85Bronchiectasis Exacerbation0.98 proportion of acute exacerbationsStandard Deviation 1.19
PlaceboBronchiectasis Exacerbation0.75 proportion of acute exacerbationsStandard Deviation 0.98
Secondary

Life Quality

(1)St George' s Respiratory Questionnaire (SGRQ); (2)Leicester Cough Questionnaire (LCQ)

Time frame: 1 year

Secondary

Lung Function

Lung function parameters: FEV1, FVC, FEV1/FVC;

Time frame: 1 year

Other Pre-specified

Rescue Medication

Use of antibiotics and rapid-acting bronchodilator

Time frame: 1 year

Source: ClinicalTrials.gov · Data processed: Mar 8, 2026