Trial Review

Please note the ANZCTR will be unattended from Friday 20 December 2024 for the holidays. The Registry will re-open on Tuesday 7 January 2025. Submissions and updates will not be processed during that time.

Registering a new trial?

To achieve prospective registration, we recommend submitting your trial for registration at the same time as ethics submission.

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been endorsed by the ANZCTR. Before participating in a study, talk to your health care provider and refer to this information for consumers
Trial registered on ANZCTR


Registration number
ACTRN12606000076572
Ethics application status
Approved
Date submitted
21/02/2006
Date registered
22/02/2006
Date last updated
2/06/2009
Type of registration
Prospectively registered

Titles & IDs
Public title
An oral killed non-typeable Haemophilus influenzae vaccine for preventing episodes of acute bronchitis in patients with mild to moderate airways disease: Safety and efficacy study
Scientific title
A multi-centre, double blind, placebo controlled, prospective study to assess safety and efficacy of orally administered killed whole cell nontypeable Haemophilus influenzae (NTHi) HI-1-164 in preventing episodes of acute bronchitis in patients with mild to moderate airway disease
Secondary ID [1] 243 0
Hunter Immunology Ltd Protocol HI-H004
Universal Trial Number (UTN)
Trial acronym
Linked study record

Health condition
Health condition(s) or problem(s) studied:
Acute bronchitis in mild to moderate airway disease 1040 0
Condition category
Condition code
Respiratory 1117 1117 0 0
Other respiratory disorders / diseases

Intervention/exposure
Study type
Interventional
Description of intervention(s) / exposure
Subjects will be randomly allocated to treatment group: active tablets containing 45mg HI-1-164-AS (inactivated non-typeable Haemophilus influenzae), Study medication (2 tablets) will be taken on days 1,2,3,29,30,31,57,58,59. The live Phase of the study will be of 8 months duration (March-October).
Intervention code [1] 912 0
Prevention
Comparator / control treatment
Placebo tablets containing excipients only.
Control group
Placebo

Outcomes
Primary outcome [1] 1491 0
Number of episodes of acute bronchitis during the study
Timepoint [1] 1491 0
During the study
Primary outcome [2] 1492 0
Proportion of subjects experiencing an episode of acute bronchitis during the study
Timepoint [2] 1492 0
During the study
Primary outcome [3] 1493 0
The duration of episodes of acute bronchitis during the study
Timepoint [3] 1493 0
During the study
Primary outcome [4] 1494 0
The number of courses of antibiotics taken for treatment of acute episodes of bronchitis during the study
Timepoint [4] 1494 0
During the study
Secondary outcome [1] 2679 0
NTHi-specific antibody
Timepoint [1] 2679 0
At beginning and end of the study
Secondary outcome [2] 2680 0
Pharyngeal colonisation with H. influenzae
Timepoint [2] 2680 0
Gargles collected at each visit, which occurred every 4 weeks (7-9 visits depending on time of registration).
Secondary outcome [3] 2681 0
Presence of H. influenzae, M. catarrhalis, S. pneumoniae and Pseudomonas spp in sputum
Timepoint [3] 2681 0
Sputum collected at each visit, which occurred every 4 weeks (7-9 visits depending on time of registration), and also during acute episodes of bronchitis.
Secondary outcome [4] 2682 0
Severity of episodes of acute bronchitis. It was planned that the analysis of the severity of episodes of acute bronchitis was to be based on the respiratory questionnaires completed by the patients at the time of each episode. However, insufficient respiratory questionnaires were completed during the study to allow for analysis of the data collected. In accordance with recent draft guidance for industry for developing drugs for treatment of COPD issued by FDA in November 2007, assessment of modification or prevention of exacerbations of disease can include severity of exacerbations as a primary efficacy endpoint. This can be based on worsening in symptoms requiring changes in treatment or requiring urgent treatment or hospitalisation. On a post hoc basis, rates of hospitalisation, corticosteroid use and a review of the medications used to treat the episodes of acute bronchitis were all analysed as measures of severity of episodes.
Timepoint [4] 2682 0
Information regarding acute episodes was collected at each visit, which occurred every 4 weeks (7-9 visits depending on time of registration).
Secondary outcome [5] 7741 0
Safety parameters. This will be assessed by collecting blood for biochemistry and haematology safety testing.
Timepoint [5] 7741 0
Bloods were collected for biochemistry and haematology safety testing at first, third and final visit.

Eligibility
Key inclusion criteria
Mild to moderate airway disease (FEV1 greater than 50% of predicted value); at least two episodes of acute bronchitis in each of the past two years; no medical or social reason for being unable to comply with the study requirements; willingness and availability to give informed consent.
Minimum age
18 Years
Maximum age
Not stated
Sex
Both males and females
Can healthy volunteers participate?
No
Key exclusion criteria
Known current chronic infection (except bronchitis); taking of antibiotics within 4 weeks prior to visit 1; participation in a clinical trial of any vaccine or immune stimulating product (except probiotics) in the past 12 months (unless known to have received placebo treatment only); participation in a clinical trial apart from that described above, in the past 3 months); pregnant, breast-feeding, or women with child-bearing potential without an effective form of contraception; any significant medical disorder which would preclude evaluation of the patient's condition (except COPD); any subject likely to withdraw or not comply with the study protocol; any other medical reason for which the investigator feels a patient should not be included.

Study design
Purpose of the study
Prevention
Allocation to intervention
Randomised controlled trial
Procedure for enrolling a subject and allocating the treatment (allocation concealment procedures)
Interested persons were mailed an Information Statement and Consent Form to read. An appointment was then made for the first visit where an informed consent discussion occurred and consent was obtained. Participants were allocated a Subject number & Randomisation number. The randomisation code was held in a sealed envelope at each study site - only randomisation code envelopes specific to that site was forwarded to the site.
Methods used to generate the sequence in which subjects will be randomised (sequence generation)
The randomisation code was generated using MS Excel. Restriction method: block randomisation
Masking / blinding
Blinded (masking used)
Who is / are masked / blinded?



Intervention assignment
Parallel
Other design features
Phase
Phase 2
Type of endpoint/s
Safety/efficacy
Statistical methods / analysis

Recruitment
Recruitment status
Completed
Date of first participant enrolment
Anticipated
7/03/2006
Actual
Date of last participant enrolment
Anticipated
Actual
Date of last data collection
Anticipated
Actual
Sample size
Target
124
Accrual to date
Final
Recruitment in Australia
Recruitment state(s)
Recruitment postcode(s) [1] 201 0
6009

Funding & Sponsors
Funding source category [1] 1221 0
Commercial sector/Industry
Name [1] 1221 0
Hunter Immunology Ltd
Country [1] 1221 0
Australia
Primary sponsor type
Commercial sector/Industry
Name
Hunter Immunology Ltd
Address
Suite 209-210, 18 Rodborough Road, Frenchs Forest, NSW 2086
Country
Australia
Secondary sponsor category [1] 1079 0
None
Name [1] 1079 0
None
Address [1] 1079 0
Country [1] 1079 0

Ethics approval
Ethics application status
Approved
Ethics committee name [1] 2553 0
Hollywood Private Hospital (Chest Clinic)
Ethics committee address [1] 2553 0
Ethics committee country [1] 2553 0
Australia
Date submitted for ethics approval [1] 2553 0
03/11/2005
Approval date [1] 2553 0
22/12/2005
Ethics approval number [1] 2553 0
HPH205

Summary
Brief summary
Trial website
Trial related presentations / publications
Public notes

Contacts
Principal investigator
Name 35866 0
Address 35866 0
Country 35866 0
Phone 35866 0
Fax 35866 0
Email 35866 0
Contact person for public queries
Name 10101 0
Emeritus Professor Robert Clancy
Address 10101 0
Hunter Immunology Ltd
Level 4, DMCSB,
Cnr King & Watt Sts,
Newcastle NSW 2300,
Australia
Country 10101 0
Australia
Phone 10101 0
+61 2 4913 8135
Fax 10101 0
+61 2 4913 8998
Email 10101 0
Robert.Clancy@newcastle.edu.au
Contact person for scientific queries
Name 1029 0
Emeritus Professor Robert Clancy
Address 1029 0
Hunter Immunology Ltd
Level 4, DMCSB,
Cnr King & Watt Sts,
Newcastle NSW 2300,
Australia
Country 1029 0
Australia
Phone 1029 0
+61 2 4913 8135
Fax 1029 0
+61 2 4913 8998
Email 1029 0
Robert.Clancy@newcastle.edu.au

No information has been provided regarding IPD availability


What supporting documents are/will be available?

No Supporting Document Provided



Results publications and other study-related documents

Documents added manually
No documents have been uploaded by study researchers.

Documents added automatically
No additional documents have been identified.