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Immunoglobulin Replacement Therapy for Immunoglobulin G Subclass 2 Deficient Patients With Bronchiectasis

Phase 4
Withdrawn
Conditions
Immunoglobulin Subclass Deficiency
Bronchiectasis
Interventions
Registration Number
NCT03737617
Lead Sponsor
University of Edinburgh
Brief Summary

Bronchiectasis is a common chronic lung condition where patients have permanent airways damage leading to daily symptoms of cough, sputum production and recurrent respiratory tract infections.

Preliminary studies in our research group have found a severe deficiency of the immune system as a rare cause of bronchiectasis (called immunoglobulin G subclass 2 deficiency) and occurs in about 1 in 20 bronchiectasis patients. The pilot work shows that these patients have more chest infections and their lung function deteriorates more rapidly.

There are no trials to date to guide doctors to decide whether we should replace this deficiency from donated blood or not. The aim with treatment is to prevent disease progression and avoid the need for long term antibiotics.

This trial will help us understand how this treatment works and its acceptability to patients. This study will help us decide whether investigators should pursue future formalised trials in many centres throughout the UK and how investigators should evaluate such a treatment.

We are looking to recruit 20 patients to this study 10 of which will receive weekly replacement therapy and the remaining 10 will receive standard care.

Detailed Description

Background What is bronchiectasis? Bronchiectasis is a chronic disabling condition due to permanently inflamed and damaged airways with patients suffering chronic cough, chronic sputum production and recurrent infections affecting 4-6 per 1,000 populations in the UK.

Causes of bronchiectasis There are a variety of causes of bronchiectasis with past infection being the commonest cause (29-42%). In about 30-53% no cause can be identified in bronchiectasis. National guidelines recommend screening for causes that are potentially treatable including immune deficiency, allergic bronchopulmonary aspergillosis, active environmental bacterial infection and cystic fibrosis as they all have therapies that may alter the disease progression.

Immunoglobulins in bronchiectasis Immunoglobulin A (IgA) and Immunoglobulin G (IgG) are the most common antibodies found in the lung, where they opsonize pathogens and protect the body from infection together with neutrophils and macrophages. Most bronchiectasis patients show higher than normal IgG and IgA antibody levels, which reflects the high degree of recurrent lung infections and chronic inflammation.

IgG has four subclasses (1-4), which bind to and opsonize different kinds of antigens. IgG2 primarily binds polysaccharides and carbohydrates that are found in bacterial capsules, the cell wall in gram-positive bacteria and the O-antigen of lipopolysaccharides found on the outer membrane of gram-negative bacteria, which makes IgG2 an important part of bacterial clearance in the lung.

The frequency of IgG2 deficiency in the general healthy population lies between 2 to 20% (N = 106). Paediatric studies show IgG2 deficiency was the most frequent IgG subclass deficiency, and in their study 10% already had bronchiectasis.

Studies to date investigating the frequency of IgG2 deficiency in bronchiectasis have been small in 56, 65 and 89 patients with IgG2 subclass deficiency varying between 5 and 29%.

Hypothesis/Rationale Immunoglobulin replacement therapy is recommended for IgG deficiency such as common variable immunodeficiency or agammaglobulinaemia to reduce infections but there is international debate whether patients with IgG subclass deficiency should be offered such treatment.

The investigators hypothesis is that IgG replacement therapy will benefit IgG2 deficient patients with bronchiectasis by reducing the bacterial burden in the airways and reducing the time to first exacerbation and reducing the overall exacerbation frequency.

STUDY DESIGN This will be an open labelled proof of concept randomised controlled trial in 20 patients- 10 will receive weekly subcutaneous IgG replacement therapy for 52 weeks and the other group no added treatment to standard care.

The technician will be blinded to the patient's treatment. The investigators have chosen the minimum patients per group to assess study feasibility and endpoints on mechanism and efficacy will help on deciding the endpoint and power of this endpoint for a future Randomised Controlled Trial (RCT).

Patients will be assessed at the following time points.

BASELINE Following confirmation of eligibility, participants will be invited to attend a baseline visit (this must take place within 8 weeks of screening).

At the baseline visit, participants will be randomised to remain on standard care alone or to receive standard care plus 52 weekly infusions of Cuvitru.

A trial diary will be provided to participant of both groups and the following assessments will be made:

* 24 hour sputum sample

* Induced sputum sample

* Lung function assessment

* Incremental Shuttle Walk Test

* Blood samples (approximately 80 ml)

* Questionnaires

* Adverse Events

* Concomitant Medications

* Sample pot provided for 24 hour sputum sample (week 26)

* Pregnancy Test (women of child bearing potential only)

For those randomised to the interventional group, weight will be measured and training will be provided to permit self-administration of the IMP at home. The first infusion of IMP will take place at the baseline visit. Weekly infusion visits will continue to take place at the Royal Infirmary of Edinburgh until the participant has been deemed competent to self-administer at home. At such time, sufficient IMP (and contingency supply) will be dispensed to permit weekly infusions until the Week 13 visit.

WEEKLY All participants will complete their diary on at least a weekly basis to record adverse events, exacerbations and concomitant medications.

Once competent, participants randomised to IgG replacement therapy will self-administer a weekly infusion of IMP at home (7±2 days following previous infusion). The date of infusion will be recorded in the diary and the vial sticker attached to document IMP use.

WEEK 13 (IgG Replacement Therapy Group Only) Participants will be asked to attend the hospital for an infusion visit 13 weeks (±2 weeks) following the baseline visit. A pregnancy test will be repeated for women of childbearing potential. Self-administration competency will be assessed during IMP infusion. Used/partially used vials of IMP and needles will be returned to the research team for destruction according to local policy. A 3 month supply of IMP (with contingency, if required) and necessary consumables will be dispensed. The completed diary will be returned to the research team and a new diary issued.

WEEK 26

Participants will attend a visit at 26 weeks (±2 weeks) following baseline. The following assessment will take place:

* 24 hour sputum sample

* Induced sputum sample

* Lung function assessment

* Incremental Shuttle Walk Test (ISWT)

* Blood samples (approximately 80 ml)

* Questionnaires

* Adverse Events

* Concomitant Medications

* Sample pot provided for 24 sputum sample (week 52)

All participants will return their completed trial diary to the research team and be issued a new one.

For participants in the IgG replacement therapy group only, self-administration competency will be assessed during IMP infusion. A pregnancy test will be repeated for women of childbearing potential. Used/partially used vials of IMP and needles will be returned to the research team for destruction according to local policy. A 3 month supply of IMP (with contingency, if required) and necessary consumables will be dispensed.

WEEK 39 (IgG Replacement Therapy Group Only) Participants will be asked to attend the hospital for an infusion visit 39 weeks (±2 weeks) following the baseline visit. A pregnancy test will be repeated for women of childbearing potential. Self-administration competency will be assessed during IMP infusion. Used/partially used vials of IMP and needles will be returned to the research team for destruction according to local policy. A 3 month supply of IMP (with contingency, if required) and necessary consumables will be dispensed. The completed diary will be returned to the research team and a new diary issued.

WEEK 52

Participants will attend the final visit at 52 weeks (or at a maximum of 54 weeks) following baseline. The following assessment will take place:

* 24 hour sputum sample

* Induced sputum sample

* Lung function assessment

* Incremental Shuttle Walk Test (ISWT)

* Blood samples (approximately 80 ml)

* Questionnaires

* Adverse Events

* Concomitant Medications

All participants will return their completed trial diary to the research team.

For participants in the IgG replacement therapy group only, all trial equipment will be returned to the research team. All used/partially used vials of IMP and needles will be returned to the research team for destruction according to local policy.

FOLLOW-UP 4 weeks (to a maximum of 5 weeks) following the 52 week visit, the research team will contact the participant by telephone to record any adverse events that have taken place since the previous visit.

This telephone call will be the last contact from the research team. Participants will then return to routine clinical care.

Recruitment & Eligibility

Status
WITHDRAWN
Sex
All
Target Recruitment
Not specified
Inclusion Criteria

Not provided

Exclusion Criteria

Not provided

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Active armCuvitru 20 % Injectable SolutionWeekly subcutaneous immunoglobulin therapy (0.1g/Kg) Cuvitru 20% Injectable Solution for 1 Year
Primary Outcome Measures
NameTimeMethod
Change in sputum bacterial load52 weeks

With IgG replacement therapy, does the sputum bacterial load change in treated versus untreated group

Proportion with bacterial load >=10(6) colony forming units/ml52 weeks

With IgG replacement therapy, does the frequency with \>=10(6) colony forming units/ml change in treated versus untreated group?

Secondary Outcome Measures
NameTimeMethod
Change of total IgG and subclasses26 and 52 weeks

Do serum IgG and subclasses change in treated versus untreated group

Change in sputum colour26 and 52 weeks

Does sputum colour change in treated versus untreated group?

Change in sputum volume26 and 52 weeks

Does 24 hour sputum volume change in treated versus untreated group

Change in sputum microbiome diversity52 weeks

Does Sputum microbiome change in treated versus untreated group

Change of forced expired volume in 1 second26 and 52 weeks

Does forced expired volume in 1 second change in treated versus untreated group

Change of forced expired volume in 1 second % predicted26 and 52 weeks

Does forced expired volume in 1 second change % predicted in treated versus untreated group

Change of forced vital capacity26 and 52 weeks

Does forced vital capacity in treated versus untreated group

Change of forced vital capacity % predicted26 and 52 weeks

Does forced vital capacity % predicted in treated versus untreated group

Change of incremental shuttle walk test26 and 52 weeks

Does the incremental shuttle walk test change in treated versus untreated group

Change of cough related quality of life using Leicester Cough Questionnaire mean score26 and 52 weeks

Does cough related quality of life change in treated versus untreated group using the Leicester Cough Questionnaire mean score (range 3-21)

Change of cough related quality of life using Leicester Cough Questionnaire with 1.3 Unit or greater improvement26 and 52 weeks

Does cough related quality of life change in treated versus untreated group using the Leicester Cough Questionnaire proportion that have 1.3 or more Unit improvement (minimum clinically important difference)

Change of quality of life using St George's Respiratory Questionnaire with 4Unit or greater improvement26 and 52 weeks

Does quality of life change in treated versus untreated group using the St George's Respiratory Questionnaire proportion that have 4 Unit or more improvement (minimum clinically important difference)

Change of quality of life using St George's Respiratory Questionnaire mean score26 and 52 weeks

Does quality of life change in treated versus untreated group using the St George's Respiratory Questionnaire mean score (range 0-100)

Change of sputum myeloperoxidase26 and 52 weeks

Does sputum myeloperoxidase change in treated versus untreated group

Change of sputum elastase26 and 52 weeks

Does sputum elastase change in treated versus untreated group

Change of sputum interleukin 826 and 52 weeks

Does sputum interleukin 8 change in treated versus untreated group

Change of serum white cell count26 and 52 weeks

Do serum white cell count change in treated versus untreated group

Change of serum C reactive protein26 and 52 weeks

Do serum C reactive protein change in treated versus untreated group

Change of serum erythrocyte sedimentation rate26 and 52 weeks

Do serum erythrocyte sedimentation rate change in treated versus untreated group

Change of serum intercellular adhesion molecule 126 and 52 weeks

Do serum intercellular adhesion molecule 1 change in treated versus untreated group

Change of phagocytosis and killing of Pseudomonas aeruginosa26 and 52 weeks

Does peripheral blood neutrophil phagocytosis and killing of Pseudomonas aeruginosa change in treated versus untreated group

Change of phagocytosis and killing of Staphylococcus aureus26 and 52 weeks

Does peripheral blood neutrophil phagocytosis and killing of Staphylococcus aureus change in treated versus untreated group

Proportion with specific antibody deficiencyBaseline

Is there antibody deficiency with pneumococcal vaccination

Time to first exacerbation requiring antibiotic therapy52 weeks

Is the time to first exacerbation requiring antibiotic therapy change in treated versus untreated group

Number of exacerbations52 weeks

Does the number of exacerbations change in treated versus untreated group

Frequency of exacerbations52 weeks

Does the mean exacerbations change in treated versus untreated group

Number of participants with side effects26 and 52 weeks

What are the number of participants with side effects of IgG therapy

Compliance rates of IgG therapy26 and 52 weeks

What are the compliance rates of IgG therapy

Completion rates of IgG therapy26 and 52 weeks

What are the completion rates of IgG therapy

Trial Locations

Locations (1)

Royal Infirmary of Edinburgh

🇬🇧

Edinburgh, United Kingdom

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